ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q32.33(chr14:106124720-106949307)x3
Germline
Classification
(1)
Benign
criteria provided, single submitter
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 |
IGHA1 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 71 | |
IGHD | - | - |
GRCh38 GRCh38 GRCh37 |
- | 71 | |
IGHD3-3 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 74 | |
IGHG1 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 70 | |
IGHG3 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 69 | |
IGHM | - | - |
GRCh38 GRCh38 GRCh37 |
1 | 88 | |
IGHV3-23 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 83 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Benign (1) |
|
Jan 7, 2015 | RCV000225198.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 13, 2023