ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q21.3-22.1(chr10:70525750-70775715)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 | |||
CCAR1 | - | - |
GRCh38 GRCh37 |
39 | 58 | |
DDX21 | - | - |
GRCh38 GRCh37 |
41 | 59 | |
DDX50 | - | - |
GRCh38 GRCh37 |
42 | 67 | |
KIFBP | - | - |
GRCh38 GRCh37 |
181 | 215 | |
STOX1 | - | - |
GRCh38 GRCh37 |
70 | 95 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
- | RCV000447949.4 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024