ClinVar Genomic variation as it relates to human health
GRCh38/hg38 Xp22.31(chrX:7847150-8460867)x0
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 | |||
LOC106029241 | - | - | - | GRCh38 | - | 167 |
LOC121627957 | - | - | - | GRCh38 | - | 163 |
LOC125446266 | - | - | - | GRCh38 | - | 172 |
LOC126863198 | - | - | - | GRCh38 | - | 180 |
LOC126863199 | - | - | - | GRCh38 | 2 | 113 |
LOC130067919 | - | - | - | GRCh38 | - | 165 |
LOC130067920 | - | - | - | GRCh38 | - | 165 |
LOC130067921 | - | - | - | GRCh38 | - | 165 |
LOC130067922 | - | - | - | GRCh38 | - | 165 |
MIR651 | - | - | - | GRCh38 | - | 157 |
There are 2 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 2, 2013 | RCV000141951.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024