ClinVar Genomic variation as it relates to human health
NC_000023.10:g.(?_109919459)_(110653626_?)del
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
CHRDL1 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
53 | 221 | |
DCX | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
283 | 450 | |
PAK3 | Some evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
175 | 348 | |
CAPN6 | - | - |
GRCh38 GRCh37 |
28 | 198 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Nov 28, 2023 | RCV004582224.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 30, 2024