ClinVar Genomic variation as it relates to human health
GRCh38/hg38 10q21.3-22.1(chr10:68543815-68977524)x1
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 | |
LOC129390195 | - | - | - | GRCh38 | - | 6 |
LOC129390196 | - | - | - | GRCh38 | - | 6 |
LOC130003947 | - | - | - | GRCh38 | - | 6 |
LOC130003948 | - | - | - | GRCh38 | - | 6 |
LOC130003949 | - | - | - | GRCh38 | - | 6 |
LOC130003950 | - | - | - | GRCh38 | - | 6 |
LOC130003951 | - | - | - | GRCh38 | - | 6 |
There are 21 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 |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Dec 22, 2010 | RCV000134927.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024