ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19q13.43(chr19:58458999-58929684)x3
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 | |||
A1BG | - | - |
GRCh38 GRCh37 |
29 | 60 | |
C19orf18 | - | - | - |
GRCh38 GRCh37 |
- | 22 |
RPS5 | - | - |
GRCh38 GRCh37 |
5 | 23 | |
ZNF135 | - | - |
GRCh38 GRCh37 |
44 | 66 | |
ZNF256 | - | - |
GRCh38 GRCh37 |
37 | 60 | |
ZNF274 | - | - |
GRCh38 GRCh37 |
8 | 28 | |
ZNF329 | - | - | - |
GRCh38 GRCh37 |
37 | 57 |
ZNF497 | - | - | - |
GRCh38 GRCh37 |
42 | 59 |
ZNF544 | - | - | - |
GRCh38 GRCh37 |
9 | 82 |
ZNF584 | - | - | - |
GRCh38 GRCh37 |
22 | 41 |
There are 6 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) |
|
Jan 20, 2016 | RCV000240566.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022