ClinVar Genomic variation as it relates to human health
NC_000009.11:g.(?_34645556)_(36277059_?)dup
Germline
Classification
(1)
Uncertain significance
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 | |||
ARHGEF39 | - | - | - |
GRCh38 GRCh37 |
24 | 115 |
ATOSB | - | - |
GRCh38 GRCh37 |
39 | 112 | |
CA9 | - | - |
GRCh38 GRCh37 |
29 | 103 | |
CCDC107 | - | - | - |
GRCh38 GRCh37 |
10 | 104 |
CCIN | - | - |
GRCh38 GRCh37 |
40 | 113 | |
CCL19 | - | - |
GRCh38 GRCh37 |
- | 82 | |
CCL21 | - | - |
GRCh38 GRCh37 |
- | 85 | |
CCL27 | - | - |
GRCh38 GRCh37 |
7 | 83 | |
CD72 | - | - |
GRCh38 GRCh37 |
17 | 91 | |
CIMIP2B | - | - | - |
GRCh38 GRCh37 |
28 | 103 |
There are 130 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 15, 2019 | RCV000708053.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023