ClinVar Genomic variation as it relates to human health
GRCh37/hg19 17q12(chr17:36972794-38033708)x4
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 | |||
ARL5C | - | - | - |
GRCh38 GRCh37 |
6 | 15 |
C17orf98 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 3 |
CACNB1 | - | - |
GRCh38 GRCh37 |
30 | 41 | |
CDK12 | - | - |
GRCh38 GRCh37 |
99 | 134 | |
CWC25 | - | - | - |
GRCh38 GRCh38 GRCh37 |
28 | 37 |
ERBB2 | - | - |
GRCh38 GRCh37 |
678 | 692 | |
FBXL20 | - | - |
GRCh38 GRCh37 |
11 | 25 | |
FBXO47 | - | - |
GRCh38 GRCh37 |
23 | 31 | |
GRB7 | - | - |
GRCh38 GRCh37 |
41 | 49 | |
IKZF3 | - | - |
GRCh38 GRCh37 |
29 | 41 |
There are 14 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 3, 2017 | RCV000683933.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022