ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19q13.43(chr19:57952073-58661581)x3
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 | |||
C19orf18 | - | - | - |
GRCh38 GRCh37 |
- | 22 |
VN1R1 | - | - |
GRCh38 GRCh37 |
22 | 42 | |
ZIK1 | - | - | - |
GRCh38 GRCh37 |
26 | 51 |
ZNF134 | - | - |
GRCh38 GRCh37 |
34 | 60 | |
ZNF135 | - | - |
GRCh38 GRCh37 |
44 | 66 | |
ZNF154 | - | - |
GRCh38 GRCh37 |
27 | 53 | |
ZNF211 | - | - |
GRCh38 GRCh37 |
26 | 57 | |
ZNF256 | - | - |
GRCh38 GRCh37 |
37 | 60 | |
ZNF329 | - | - | - |
GRCh38 GRCh37 |
37 | 57 |
ZNF416 | - | - | - |
GRCh38 GRCh37 |
27 | 52 |
There are 21 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) |
|
Dec 15, 2017 | RCV000846105.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022