ClinVar Genomic variation as it relates to human health
GRCh37/hg19 19p13.11-12(chr19:19903805-21966609)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 | |||
ZNF100 | - | - |
GRCh38 GRCh38 GRCh37 |
43 | 59 | |
ZNF253 | - | - |
GRCh38 GRCh37 |
28 | 42 | |
ZNF429 | - | - | - |
GRCh38 GRCh37 |
48 | 60 |
ZNF430 | - | - | - |
GRCh38 GRCh38 GRCh37 |
27 | 42 |
ZNF431 | - | - |
GRCh38 GRCh37 |
31 | 48 | |
ZNF486 | - | - | - |
GRCh38 GRCh37 |
60 | 76 |
ZNF493 | - | - | - |
GRCh38 GRCh37 |
58 | 69 |
ZNF506 | - | - | - |
GRCh38 GRCh37 |
27 | 40 |
ZNF626 | - | - | - |
GRCh38 GRCh37 |
39 | 58 |
ZNF682 | - | - | - |
GRCh38 GRCh37 |
29 | 44 |
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) |
|
Feb 28, 2018 | RCV000684092.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022