ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Yp11.2-q11.222(chrY:6255441-18435984)x2
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 | |||
AMELY | - | - |
GRCh38 GRCh37 |
1 | 78 | |
CDY2A | - | - |
GRCh38 GRCh37 |
1 | 82 | |
CDY2B | - | - | - | GRCh38 | - | 35 |
DDX3Y | - | - |
GRCh38 GRCh37 |
5 | 75 | |
FAM197Y1P | - | - | - | GRCh37 | - | 56 |
FAM197Y2 | - | - | - |
GRCh38 GRCh38 |
- | 22 |
FAM197Y3 | - | - | - |
GRCh38 GRCh38 |
- | 22 |
FAM197Y4 | - | - | - |
GRCh38 GRCh38 |
- | 22 |
FAM197Y5 | - | - | - |
GRCh38 GRCh38 |
- | 22 |
FAM197Y6 | - | - | - |
GRCh38 GRCh38 |
- | 22 |
There are 53 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Pathogenic (1) |
|
May 30, 2010 | RCV000134034.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024