ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19q13.12-13.2(chr19:36685995-38708166)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 | |||
DPF1 | - | - |
GRCh38 GRCh37 |
7 | 24 | |
SIPA1L3 | - | - |
GRCh38 GRCh37 |
350 | 368 | |
WDR87 | - | - |
GRCh38 GRCh37 |
330 | 348 | |
ZFP14 | - | - |
GRCh38 GRCh37 |
23 | 39 | |
ZFP30 | - | - |
GRCh38 GRCh37 |
24 | 40 | |
ZFP82 | - | - | - |
GRCh38 GRCh37 |
19 | 35 |
ZNF146 | - | - |
GRCh38 GRCh37 |
- | 21 | |
ZNF260 | - | - |
GRCh38 GRCh37 |
27 | 43 | |
ZNF345 | - | - | - |
GRCh38 GRCh37 |
10 | 62 |
ZNF382 | - | - |
GRCh38 GRCh37 |
25 | 41 |
There are 23 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) |
|
Jul 20, 2015 | RCV000207200.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 14, 2024