Variant #0001059399 (NC_000007.13:g.(?_154537776)_(159125464_?)del)

Individual ID 00469594
Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.(?_154537776)_(159125464_?)del
DNA change (hg38) g.?
Published as arr[hg19] 7q36.2q36.3(154,537,776-159,125,464)x1
ISCN -
DB-ID chr7_007599
Variant remarks -
Reference PubMed: Retterer 2016
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2025-11-18 12:45:53 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000471262 DNA arrayCGH - - - 2 Johan den Dunnen


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.