ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Yq11.222-11.223(chrY:18664321-22358529)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 | |||
EIF1AY | - | - |
GRCh38 GRCh37 |
- | 79 | |
FAM197Y10 | - | - | - | GRCh37 | - | 79 |
HSFY2 | - | - | - |
GRCh38 GRCh37 |
1 | 88 |
KDM5D | - | - |
GRCh38 GRCh37 |
- | 78 | |
LOC106144610 | - | - | - |
GRCh38 GRCh38 |
- | 30 |
LOC126057109 | - | - | - | GRCh38 | - | 29 |
LOC126057110 | - | - | - | GRCh38 | - | 29 |
LOC126057111 | - | - | - | GRCh38 | - | 29 |
LOC126057112 | - | - | - | GRCh38 | - | 29 |
LOC126057113 | - | - | - | GRCh38 | - | 29 |
There are 15 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
|
Uncertain significance (1) |
|
Dec 22, 2010 | RCV000142769.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024