Variant #0001070241 (NC_000006.11:g.19066298_21763281inv)

Individual ID 00474045
Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic (dominant)
DNA change (genomic) (Relative to hg19 / GRCh37) g.19066298_21763281inv
DNA change (hg38) g.19066067_21763050inv
Published as g.19066067_21763050inv
ISCN -
DB-ID chr6_008321
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Elsa Lucas Castro
Database submission license No license selected
Created by Elsa Lucas Castro
Date created 2026-03-09 10:33:37 +01:00 (CET)
Date last edited 2026-03-30 15:22:51 +02:00 (CEST)
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Variant on transcripts

Stop! No variants on transcripts found!



Screenings


AscendingScreening ID     

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Owner     
0000475715 DNA SEQ-NG Blood WGS - 1 Elsa Lucas Castro


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