ClinVar Genomic variation as it relates to human health
GRCh37/hg19 Yq11.21-11.221(chrY:14844481-16824498)x0
Germline
Classification
(1)
Pathogenic
no assertion criteria provided
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 | |||
DDX3Y | - | - |
GRCh38 GRCh37 |
5 | 75 | |
NLGN4Y | - | - |
GRCh38 GRCh37 |
10 | 82 | |
TMSB4Y | - | - |
GRCh38 GRCh37 |
2 | 65 | |
USP9Y | - | - |
GRCh38 GRCh37 |
17 | 92 | |
UTY | - | - |
GRCh38 GRCh37 |
3 | 68 | |
VCY | - | - |
GRCh38 GRCh37 |
2 | 65 | |
VCY1B | - | - |
GRCh38 GRCh37 |
4 | 68 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
Oct 21, 2014 | RCV000510338.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024