ClinVar Genomic variation as it relates to human health
GRCh38/hg38 14q32.33(chr14:106467689-106774412)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 |
IGHV1-45 | - | - | - |
GRCh38 GRCh38 |
- | 47 |
IGHV1-46 | - | - | - |
GRCh38 GRCh38 |
- | 47 |
IGHV1-58 | - | - | - |
GRCh38 GRCh38 |
- | 49 |
IGHV1-69 | - | - | - |
GRCh38 GRCh38 |
- | 62 |
IGHV1-69-2 | - | - | - |
GRCh38 GRCh38 |
- | 62 |
IGHV1-69D | - | - | - |
GRCh38 GRCh38 |
- | 62 |
IGHV2-70 | - | - | - |
GRCh38 GRCh38 |
- | 61 |
IGHV2-70D | - | - | - |
GRCh38 GRCh38 |
- | 62 |
IGHV3-43 | - | - | - |
GRCh38 GRCh38 |
- | 47 |
There are 9 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 |
---|---|---|---|---|
Benign (1) |
|
Sep 21, 2012 | RCV000142493.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024