ClinVar Genomic variation as it relates to human health
GRCh37/hg19 14q32.33(chr14:105814886-107285437)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 | |||
CRIP1 | - | - |
GRCh38 GRCh37 |
13 | 91 | |
CRIP2 | - | - |
GRCh38 GRCh37 |
20 | 97 | |
IGH |
|
- | - |
GRCh38 GRCh38 GRCh37 |
10 | 180 |
IGHA1 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 72 | |
IGHA2 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 71 | |
IGHD | - | - |
GRCh38 GRCh38 GRCh37 |
- | 72 | |
IGHD3-3 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 75 | |
IGHE | - | - |
GRCh38 GRCh38 GRCh37 |
- | 73 | |
IGHG1 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 71 | |
IGHG2 | - | - |
GRCh38 GRCh38 GRCh37 |
- | 75 |
There are 9 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Feb 5, 2015 | RCV000511369.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024