ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10p15.1-14(chr10:4927427-6653936)x3
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 | |||
AKR1C1 | - | - |
GRCh38 GRCh37 |
28 | 69 | |
AKR1C2 | - | - |
GRCh38 GRCh37 |
82 | 131 | |
AKR1C3 | - | - |
GRCh38 GRCh37 |
27 | 69 | |
AKR1C4 | - | - |
GRCh38 GRCh37 |
67 | 104 | |
ANKRD16 | - | - |
GRCh38 GRCh37 |
21 | 59 | |
ASB13 | - | - |
GRCh38 GRCh37 |
13 | 47 | |
CALML3 | - | - |
GRCh38 GRCh37 |
- | 44 | |
CALML3-AS1 | - | - | - |
GRCh38 GRCh37 |
- | 44 |
CALML5 | - | - |
GRCh38 GRCh37 |
7 | 42 | |
FBH1 | - | - |
GRCh38 GRCh37 |
56 | 98 |
There are 10 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Mar 1, 2021 | RCV001827671.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022