ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q24.32-24.33(chr10:104883845-105482700)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 | |||
ATP5MK | - | - |
GRCh38 GRCh37 |
7 | 34 | |
CALHM1 | - | - |
GRCh38 GRCh37 |
30 | 57 | |
CALHM2 | - | - |
GRCh38 GRCh37 |
30 | 57 | |
CALHM3 | - | - |
GRCh38 GRCh37 |
28 | 54 | |
INA | - | - |
GRCh38 GRCh37 |
29 | 54 | |
NEURL1 | - | - |
GRCh38 GRCh37 |
46 | 71 | |
NT5C2 | - | - |
GRCh38 GRCh37 |
203 | 264 | |
PCGF6 | - | - |
GRCh38 GRCh37 |
22 | 49 | |
PDCD11 | - | - |
GRCh38 GRCh37 |
108 | 135 | |
SH3PXD2A | - | - |
GRCh38 GRCh37 |
85 | 109 |
There is 1 more gene 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) |
|
Nov 27, 2019 | RCV001258465.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022