Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Template: Template(s) used to detect the sequence variant; DNA (genomic DNA), RNA (cDNA) or protein
All options:
- DNA
- RNA = RNA (cDNA)
- protein
- ? = unknown
Technique: technique(s) used to identify the sequence variant.
All options:
- ? = unknown
- ARMS = amplification refractory mutation system
- arrayCGH = array for Comparative Genomic Hybridisation
- arrayMET = array for methylation analysis
- arraySEQ = array for resequencing
- arraySNP = array for SNP typing
- arrayCNV = array for Copy Number Variation (SNP and CNV probes)
- ASO = allele-specific oligo hybridisation
- BESS = Base Excision Sequence Scanning
- CMC = Chemical Mismatch Cleavage
- COBRA = Combined Bisulfite Restriction Analysis
- CSCE = Conformation Sensitive Capillary Electrophoresis
- CSGE = Conformation Sensitive Gel Electrophoresis
- ddF = dideoxy Fingerprinting
- DGGE = Denaturing-Gradient Gel-Electrophoresis
- DHPLC = Denaturing High-Performance Liquid Chromatography
- DOVAM = Detection Of Virtually All Mutations (SSCA variant)
- DSCA = Double-Strand DNA Conformation Analysis
- DSDI = Detection Small Deletions and Insertions
- EMC = Enzymatic Mismatch Cleavage
- expr = expression analysis
- FISH = Fluorescent In-Situ Hybridisation
- FISHf = fiberFISH
- HD = HeteroDuplex analysis
- HPLC = High-Performance Liquid Chromatography
- IEF = IsoElectric Focussing
- IHC = Immuno-Histo-Chemistry
- Invader = Invader assay
- MAPH = Multiplex Amplifiable Probe Hybridisation
- MAQ = Multiplex Amplicon Quantification
- MCA = Melting Curve Analysis, high-resolution (HRMA)
- microscope = microscopic analysis (karyotype)
- microsat = microsatellite genotyping
- minigene = expression minigene construct
- MIP = Molecular Inversion Probe amplification
- MIPsm = single molecule Molecular Inversion Probe amplification
- MLPA = Multiplex Ligation-dependent Probe Amplification
- MLPA-ms = Multiplex Ligation-dependent Probe Amplification, methylation specific
- MS = mass spectrometry
- Northern = Northern blotting
- NUC = nuclease digestion (RNAseT1, S1)
- OM = optical mapping
- PAGE = Poly-Acrylamide Gel-Electrophoresis
- PCR = Polymerase Chain Reaction
- PCRdd = PCR, digital droplet
- PCRdig = PCR + restriction enzyme digestion
- PCRh = PCR, haloplex
- PCRlr = PCR, long-range
- PCRm = PCR, multiplex
- PCRms = PCR, methylation sensitive
- PCRq = PCR, quantitative (qPCR)
- PCRrp = PCR, repeat-primed (RP-PCR)
- PCRsqd = PCR, semi-quantitative duplex
- PE = primer extension (APEX, SNaPshot)
- PEms = primer extension, methylation-sensitive single-nucleotide
- PFGE = Pulsed-Field Gel-Electrophoresis (+Southern)
- PTT = Protein Truncation Test
- RFLP = Restriction Fragment Length Polymorphisms
- RT-PCR = Reverse Transcription and PCR
- RT-PCRq = Reverse Transcription and PCR, quantitative
- SBE = Single Base Extension
- SEQ = SEQuencing (Sanger)
- SEQb = bisulfite SEQuencing
- SEQp = pyroSequencing
- SEQms = sequencing, methylation specific
- SEQ-ON = next-generation sequencing - Oxford Nanopore
- SEQ-NG = next-generation sequencing
- SEQ-NG-RNA = next-generation sequencing RNA
- SEQ-NG-H = next-generation sequencing - Helicos
- SEQ-NG-I = next-generation sequencing - Illumina/Solexa
- SEQ-NG-IT = next-generation sequencing - Ion Torrent
- SEQ-NG-R = next-generation sequencing - Roche/454
- SEQ-NG-S = next-generation sequencing - SOLiD
- SEQ-PB = next-generation sequencing - Pacific Biosciences
- SNPlex = SNPlex
- Southern = Southern blotting
- SSCA = Single-Strand DNA Conformation polymorphism Analysis (SSCP)
- SSCAf = fluorescent SSCA (SSCP)
- STR = Short Tandem Repeat
- TaqMan = TaqMan assay
- Western = Western blotting
- - = not applicable
Tissue: tissue type used for analysis
Remarks: remarks regarding the screening like WGS (whole genome sequencing), WES (whole exome sequencing, gene panel (incl. a list of genes analysed), etc.
How to query this table
All list views have search fields which can be used to search data.
You can search for a complete word or you can search for a part of a search term.
If you enclose two or more words in double quotes, LOVD will search for the combination of those words only exactly in the order you specify.
Note that search terms are case-insensitive and that wildcards such as * are treated as normal text!
For all options, like "and", "or", and "not" searches, or searching for prefixes or suffixes, see the table below.
Operator |
Column type |
Example |
Matches |
|
Text |
Arg |
all entries containing 'Arg' |
space |
Text |
Arg Ser |
all entries containing 'Arg' and 'Ser' |
| |
Text |
Arg|Ser |
all entries containing 'Arg' or 'Ser' |
! |
Text |
!fs |
all entries not containing 'fs' |
^ |
Text |
^p.(Arg |
all entries beginning with 'p.(Arg' |
$ |
Text |
Ser)$ |
all entries ending with 'Ser)' |
="" |
Text |
="" |
all entries with this field empty |
="" |
Text |
="p.0" |
all entries exactly matching 'p.0' |
!="" |
Text |
!="" |
all entries with this field not empty |
!="" |
Text |
!="p.0" |
all entries not exactly matching 'p.0?' |
combination |
Text |
*|Ter !fs |
all entries containing '*' or 'Ter' but not containing 'fs' |
|
Date |
2020 |
all entries matching the year 2020 |
| |
Date |
2020-03|2020-04 |
all entries matching March or April, 2020 |
! |
Date |
!2020-03 |
all entries not matching March, 2020 |
< |
Date |
<2020 |
all entries before the year 2020 |
<= |
Date |
<=2020-06 |
all entries in or before June, 2020 |
> |
Date |
>2020-06 |
all entries after June, 2020 |
>= |
Date |
>=2020-06-15 |
all entries on or after June 15th, 2020 |
combination |
Date |
2019|2020 <2020-03 |
all entries in 2019 or 2020, and before March, 2020 |
|
Numeric |
23 |
all entries exactly matching 23 |
| |
Numeric |
23|24 |
all entries exactly matching 23 or 24 |
! |
Numeric |
!23 |
all entries not exactly matching 23 |
< |
Numeric |
<23 |
all entries lower than 23 |
<= |
Numeric |
<=23 |
all entries lower than, or equal to, 23 |
> |
Numeric |
>23 |
all entries higher than 23 |
>= |
Numeric |
>=23 |
all entries higher than, or equal to, 23 |
combination |
Numeric |
>=20 <30 !23 |
all entries with values from 20 to 29, but not equal to 23 |
Some more advanced examples:
Example |
Matches |
Asian |
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc. |
Asian !Caucasian |
all entries containing 'Asian' but not containing 'Caucasian' |
Asian|African !Caucasian |
all entries containing 'Asian' or 'African', but not containing 'Caucasian' |
"South Asian" |
all entries containing 'South Asian', but not containing 'South East Asian' |
To sort on a certain column, click on the column header or on the arrows.
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The column currently sorted on has a darker blue background color than the other columns.
The up and down arrows next to the column name indicate the current sorting direction.
When sorting on any field other than the default, LOVD will sort secondarily on the default sort column.
|
Legend |
How to query |
« First |
Prev |
|
1 |
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Next |
Last » |

 Screening ID
|

 Individual ID
|

 Template
|

 Technique
|

 Tissue
|
 Remarks
|

 Variants found
|

 Owner
|
0000309522 |
00308378 |
DNA |
SEQ;SEQ-NG |
- |
123 gene panel |
1 |
Global Variome, with Curator vacancy |
0000309541 |
00308397 |
DNA |
SEQ;SEQ-NG |
- |
123 gene panel |
1 |
Global Variome, with Curator vacancy |
0000309542 |
00308398 |
DNA |
SEQ;SEQ-NG |
- |
123 gene panel |
2 |
Global Variome, with Curator vacancy |
0000309807 |
00308662 |
DNA |
SEQ;SEQ-NG |
- |
204 gene panel |
2 |
Global Variome, with Curator vacancy |
0000310440 |
00309295 |
DNA |
SEQ |
- |
- |
1 |
Global Variome, with Curator vacancy |
0000310441 |
00309296 |
DNA |
SEQ |
- |
- |
1 |
Global Variome, with Curator vacancy |
0000329184 |
00327969 |
DNA |
SEQ-NG |
- |
WGS |
1 |
LOVD |
0000329332 |
00328117 |
DNA |
SEQ-NG |
- |
WGS |
2 |
LOVD |
0000329465 |
00328250 |
DNA |
SEQ-NG |
- |
WGS |
1 |
LOVD |
0000332946 |
00331727 |
DNA |
SEQ |
- |
- |
1 |
LOVD |
0000333500 |
00332280 |
DNA |
SEQ-NG |
- |
300-gene panel |
1 |
LOVD |
0000333693 |
00332469 |
DNA |
SEQ-NG |
- |
150-gene panel |
1 |
LOVD |
0000336454 |
00335225 |
DNA |
SEQ-NG |
- |
212-gene panel |
1 |
LOVD |
0000363373 |
00362144 |
DNA |
SEQ-NG |
- |
WES |
2 |
Johan den Dunnen |
0000363374 |
00362145 |
DNA |
SEQ-NG |
- |
WES |
1 |
Johan den Dunnen |
0000363375 |
00362146 |
DNA |
SEQ-NG |
- |
WES |
2 |
Johan den Dunnen |
0000364153 |
00362925 |
DNA |
SEQ-NG |
- |
WES |
2 |
LOVD |
0000364602 |
00363374 |
DNA |
SEQ-NG |
- |
WES |
1 |
LOVD |
0000364834 |
00363606 |
DNA |
SEQ-NG |
- |
gene panel |
1 |
LOVD |
0000364860 |
00363632 |
DNA |
SEQ-NG |
- |
gene panel |
1 |
LOVD |
0000364925 |
00363697 |
DNA |
SEQ-NG |
- |
gene panel |
1 |
LOVD |
0000379209 |
00378005 |
DNA |
PCR; SEQ |
blood |
- |
1 |
LOVD |
0000379210 |
00378006 |
DNA |
PCR; SEQ |
blood |
- |
1 |
LOVD |
0000382068 |
00380854 |
DNA |
SEQ-NG |
blood |
Whole-exome sequencing |
1 |
LOVD |
0000382073 |
00380859 |
DNA |
SEQ-NG |
blood |
Whole-exome sequencing |
1 |
LOVD |
0000382357 |
00381142 |
DNA |
SEQ |
blood |
- |
1 |
Martin Zenker, Prof. Dr. med. |
0000384733 |
00383508 |
DNA |
SEQ-NG-I |
blood |
204 genes associated with inherited retinal disorders; see paper |
2 |
LOVD |
0000385437 |
00384212 |
DNA |
SEQ-NG-I |
blood |
108-gene panel targeted resequencing using MIPs library prep |
1 |
LOVD |
0000385678 |
00384453 |
DNA |
SEQ-NG |
blood |
panel of 126 genes |
1 |
LOVD |
0000391024 |
00389781 |
DNA |
SEQ-NG |
blood |
RET7 targeted sequencing panel - see paper |
1 |
LOVD |
0000391160 |
00389917 |
DNA |
SEQ-NG |
blood |
RET8 targeted sequencing panel - see paper |
1 |
LOVD |
0000391161 |
00389918 |
DNA |
SEQ |
blood |
Sanger sequencing |
1 |
LOVD |
0000391227 |
00389984 |
DNA |
SEQ-NG |
blood |
RET8 targeted sequencing panel - see paper |
1 |
LOVD |
0000391581 |
00390340 |
DNA |
SEQ-NG-I |
blood |
whole genome sequencing |
1 |
LOVD |
0000391582 |
00390341 |
DNA |
SEQ-NG-I |
blood |
whole genome sequencing |
2 |
LOVD |
0000391583 |
00390342 |
DNA |
SEQ-NG-I |
blood |
whole genome sequencing |
1 |
LOVD |
0000392196 |
00390955 |
DNA |
SEQ |
- |
- |
2 |
LOVD |
0000392623 |
00391381 |
DNA |
SEQ-NG |
- |
retrospective case note review, targeted gene panel testing |
1 |
LOVD |
0000393165 |
00391923 |
DNA |
SEQ-NG |
blood |
Whole-exome or targeted sequencing |
2 |
LOVD |
0000393166 |
00391924 |
DNA |
SEQ-NG |
blood |
Whole-exome or targeted sequencing |
2 |
LOVD |
0000393167 |
00391925 |
DNA |
SEQ-NG |
blood |
Whole-exome or targeted sequencing |
2 |
LOVD |
0000393168 |
00391926 |
DNA |
SEQ-NG |
blood |
Whole-exome or targeted sequencing |
2 |
LOVD |
0000393169 |
00391927 |
DNA |
SEQ-NG |
blood |
Whole-exome or targeted sequencing |
2 |
LOVD |
0000393170 |
00391928 |
DNA |
SEQ-NG |
blood |
Whole-exome or targeted sequencing |
1 |
LOVD |
0000393171 |
00391929 |
DNA |
SEQ-NG |
blood |
Whole-exome or targeted sequencing |
2 |
LOVD |
0000395233 |
00393985 |
DNA |
PCR;SEQ |
blood |
- |
2 |
LOVD |
0000400015 |
00398774 |
DNA |
SEQ-NG |
- |
tagreted next-generation sequencing |
2 |
LOVD |
0000417339 |
00416059 |
DNA |
arraySNP;SEQ |
blood |
- |
1 |
LOVD |
0000417340 |
00416060 |
DNA |
arraySNP;SEQ |
blood |
- |
1 |
LOVD |
0000417341 |
00416061 |
DNA |
arraySNP;SEQ |
blood |
- |
1 |
LOVD |
0000417342 |
00416062 |
DNA |
arraySNP;SEQ |
blood |
- |
1 |
LOVD |
0000417343 |
00416063 |
DNA |
SEQ |
blood |
- |
2 |
LOVD |
0000417344 |
00416064 |
DNA |
SEQ |
blood |
- |
2 |
LOVD |
0000417345 |
00416065 |
DNA |
SEQ |
blood |
- |
2 |
LOVD |
0000417388 |
00416108 |
DNA |
SEQ |
blood |
- |
2 |
LOVD |
0000417389 |
00416109 |
DNA |
SEQ |
blood |
- |
2 |
LOVD |
0000417390 |
00416110 |
DNA |
SEQ |
blood |
- |
2 |
LOVD |
0000417391 |
00416111 |
DNA |
SEQ |
blood |
- |
2 |
LOVD |
0000417392 |
00416112 |
DNA |
SEQ |
blood |
- |
2 |
LOVD |
0000417393 |
00416113 |
DNA |
SEQ |
blood |
- |
1 |
LOVD |
0000417394 |
00416115 |
DNA |
SEQ |
blood |
- |
2 |
LOVD |
0000417395 |
00416116 |
DNA |
SEQ |
blood |
- |
1 |
LOVD |
0000417396 |
00416117 |
DNA |
SEQ |
blood |
- |
1 |
LOVD |
0000417397 |
00416118 |
DNA |
SEQ |
blood |
- |
1 |
LOVD |
0000417398 |
00416119 |
DNA |
SEQ |
blood |
- |
1 |
LOVD |
0000417399 |
00416120 |
DNA |
SEQ |
blood |
- |
1 |
LOVD |
0000417401 |
00416122 |
DNA |
SEQ |
blood |
whole-exome sequencing, also in mother and father |
1 |
LOVD |
0000417402 |
00416123 |
DNA |
SEQ |
blood |
whole-exome sequencing, also in mother and father |
1 |
LOVD |
0000417408 |
00416129 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
1 |
LOVD |
0000417409 |
00416130 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
1 |
LOVD |
0000417410 |
00416131 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
2 |
LOVD |
0000417411 |
00416132 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
1 |
LOVD |
0000417412 |
00416133 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
2 |
LOVD |
0000417413 |
00416134 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
1 |
LOVD |
0000417414 |
00416135 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
1 |
LOVD |
0000417415 |
00416136 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
1 |
LOVD |
0000417416 |
00416137 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
2 |
LOVD |
0000417417 |
00416138 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
1 |
LOVD |
0000417418 |
00416139 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
2 |
LOVD |
0000417419 |
00416140 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
2 |
LOVD |
0000417420 |
00416141 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
1 |
LOVD |
0000417421 |
00416142 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
1 |
LOVD |
0000417422 |
00416143 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
1 |
LOVD |
0000417423 |
00416144 |
DNA |
SEQ-NG;SEQ |
blood |
targeted next generation sequencing |
2 |
LOVD |
0000417471 |
00416192 |
DNA |
SEQ-NG;SEQ |
blood |
whole-exome sequencing |
1 |
LOVD |
0000417473 |
00416194 |
DNA |
SEQ-NG;SEQ |
- |
176 genes associated with retinal dystrophy, panel next-generation sequencing |
2 |
LOVD |
0000417474 |
00416195 |
DNA |
SEQ-NG;SEQ |
- |
176 genes associated with retinal dystrophy, panel next-generation sequencing |
1 |
LOVD |
0000417475 |
00416196 |
DNA |
SEQ-NG;SEQ |
- |
176 genes associated with retinal dystrophy, panel next-generation sequencing |
1 |
LOVD |
0000417476 |
00416197 |
DNA |
SEQ-NG;SEQ |
- |
176 genes associated with retinal dystrophy, panel next-generation sequencing |
2 |
LOVD |
0000417477 |
00416198 |
DNA |
SEQ-NG;SEQ |
- |
176 genes associated with retinal dystrophy, panel next-generation sequencing |
1 |
LOVD |
0000417478 |
00416199 |
DNA |
SEQ-NG;SEQ |
- |
176 genes associated with retinal dystrophy, panel next-generation sequencing |
1 |
LOVD |
0000417479 |
00416200 |
DNA |
SEQ-NG;SEQ |
- |
176 genes associated with retinal dystrophy, panel next-generation sequencing |
2 |
LOVD |
0000424545 |
00423235 |
DNA |
SEQ-NG;SEQ |
- |
panel next-generation sequencing |
2 |
LOVD |
0000424546 |
00423236 |
DNA |
SEQ-NG;SEQ |
- |
panel next-generation sequencing |
2 |
LOVD |
0000424547 |
00423237 |
DNA |
SEQ |
- |
- |
2 |
LOVD |
0000424548 |
00423238 |
DNA |
SEQ |
- |
- |
1 |
LOVD |
0000424549 |
00423239 |
DNA |
SEQ-NG;SEQ |
- |
whole exome sequencing |
1 |
LOVD |
0000424550 |
00423240 |
DNA |
SEQ-NG;SEQ |
- |
next-generation sequencing achromatopsia 6 genes panel |
2 |
LOVD |
0000424551 |
00423241 |
DNA |
SEQ-NG;SEQ |
- |
next-generation sequencing achromatopsia 6 genes panel |
1 |
LOVD |
0000424552 |
00423242 |
DNA |
SEQ-NG;SEQ |
- |
next-generation sequencing retinal dystrophy 325 genes panel |
1 |
LOVD |
|
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How to query |
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