ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q32.3(chr14:106252705-106538480)x1
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 | |||
FAM30A | - | - |
GRCh38 GRCh38 |
- | 36 | |
IGH |
|
- | - |
GRCh38 GRCh38 GRCh37 |
10 | 179 |
IGHA1 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 71 | |
IGHD | - | - |
GRCh38 GRCh38 GRCh37 |
- | 71 | |
IGHD1-1 | - | - | - |
GRCh38 GRCh38 |
- | 36 |
IGHD1-14 | - | - | - |
GRCh38 GRCh38 |
- | 36 |
IGHD1-20 | - | - | - |
GRCh38 GRCh38 |
- | 36 |
IGHD1-26 | - | - | - |
GRCh38 GRCh38 |
- | 36 |
IGHD1-7 | - | - | - |
GRCh38 GRCh38 |
- | 38 |
IGHD2-15 | - | - | - |
GRCh38 GRCh38 |
- | 36 |
There are 44 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) |
|
Aug 12, 2011 | RCV000051222.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024