ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Yq11.223-11.23(chrY:23127722-24882383)x0
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 | |||
DAZ1 | No evidence available | No evidence available |
GRCh38 GRCh37 |
- | 99 | |
BPY2B | - | - | - |
GRCh38 GRCh37 |
- | 102 |
CDY1B | - | - | - | GRCh38 | - | 31 |
DAZ2 | - | - |
GRCh38 GRCh37 |
- | 98 | |
DAZ3 | - | - |
GRCh38 GRCh37 |
- | 102 | |
DAZ4 | - | - |
GRCh38 GRCh37 |
- | 103 | |
LOC106144557 | - | - | - | GRCh38 | 1 | 32 |
TTTY17B | - | - | - |
GRCh38 GRCh37 |
- | 102 |
TTTY3B | - | - | - |
GRCh38 GRCh37 |
- | 98 |
TTTY4B | - | - | - |
GRCh38 GRCh37 |
- | 102 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Likely benign (1) |
|
- | RCV000141537.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024