ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Yq11.221(chrY:12787777-13548311)x2
Germline
Classification
(1)
Uncertain significance
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 | |
LOC108004538 | - | - | - | GRCh38 | - | 26 |
MIR12120 | - | - | - | GRCh38 | - | 24 |
USP9Y | - | - |
GRCh38 GRCh37 |
17 | 92 | |
UTY | - | - |
GRCh38 GRCh37 |
3 | 68 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Sep 27, 2013 | RCV000140760.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024