ClinVar Genomic variation as it relates to human health
GRCh37/hg19 5p14.3-13.3(chr5:19324003-30115028)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 | |||
CDH10 | - | - |
GRCh38 GRCh37 |
42 | 98 | |
CDH12 | - | - |
GRCh38 GRCh37 |
80 | 153 | |
CDH18 | - | - |
GRCh38 GRCh37 |
60 | 132 | |
CDH9 | - | - |
GRCh38 GRCh37 |
48 | 95 | |
LINC02899 | - | - | - |
GRCh38 GRCh37 |
- | 57 |
PRDM9 | - | - |
GRCh38 GRCh38 GRCh37 |
83 | 142 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Nov 26, 2019 | RCV001258686.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022