ClinVar Genomic variation as it relates to human health
GRCh37/hg19 2q35(chr2:219221864-219423299)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 | |||
CATIP | - | - |
GRCh38 GRCh37 |
4 | 56 | |
CTDSP1 | - | - |
GRCh38 GRCh37 |
21 | 50 | |
MIR26B | - | - |
GRCh38 GRCh37 |
- | 29 | |
SLC11A1 | - | - |
GRCh38 GRCh37 |
80 | 109 | |
USP37 | - | - |
GRCh38 GRCh37 |
43 | 73 | |
VIL1 | - | - |
GRCh38 GRCh37 |
72 | 102 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Jul 20, 2015 | RCV000207108.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 14, 2024