ClinVar Genomic variation as it relates to human health
GRCh37/hg19 13q31.3(chr13:91209639-94704856)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 | |||
GPC5 | No evidence available | No evidence available |
GRCh38 GRCh37 |
72 | 159 | |
GPC6 | - | - |
GRCh38 GRCh37 |
272 | 412 | |
MIR17 | - | - |
GRCh38 GRCh37 |
- | 85 | |
MIR17HG | - | - |
GRCh38 GRCh37 |
21 | 106 | |
MIR18A | - | - |
GRCh38 GRCh37 |
- | 85 | |
MIR19A | - | - |
GRCh38 GRCh37 |
- | 85 | |
MIR19B1 | - | - |
GRCh38 GRCh37 |
- | 85 | |
MIR20A | - | - |
GRCh38 GRCh37 |
- | 85 | |
MIR92A1 | - | - |
GRCh38 GRCh37 |
- | 85 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Jan 20, 2016 | RCV000240035.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022