ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Yq11.21-11.221(chrY:12084990-12742051)x2
Germline
Classification
(1)
Likely benign
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 | |||
LOC106128902 | - | - | - | GRCh38 | 1 | 24 |
TTTY15 | - | - | - |
GRCh38 GRCh37 |
1 | 72 |
USP9Y | - | - |
GRCh38 GRCh37 |
17 | 92 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
Jun 1, 2012 | RCV000137360.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024