ClinVar Genomic variation as it relates to human health
GRCh38/hg38 14q32.33(chr14:106623930-106689692)x3
Germline
Classification
(1)
Benign
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 | |||
IGH |
|
- | - |
GRCh38 GRCh38 GRCh37 |
10 | 179 |
IGHV3-64 | - | - | - |
GRCh38 GRCh38 |
- | 48 |
IGHV3-66 | - | - | - |
GRCh38 GRCh38 |
- | 47 |
IGHV4-59 | - | - | - |
GRCh38 GRCh38 |
- | 53 |
IGHV4-61 | - | - | - |
GRCh38 GRCh38 |
- | 51 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Jun 30, 2010 | RCV000142436.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024