ClinVar Genomic variation as it relates to human health
chr20:60885242-61929348 complex variant
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 | |||
ARFGAP1 | - | - |
GRCh38 GRCh37 |
37 | 107 | |
BHLHE23 | - | - |
GRCh38 GRCh37 |
6 | 56 | |
BIRC7 | - | - |
GRCh38 GRCh37 |
22 | 87 | |
CABLES2 | - | - |
GRCh38 GRCh37 |
31 | 70 | |
COL20A1 | - | - |
GRCh38 GRCh37 |
113 | 183 | |
COL9A3 | - | - |
GRCh38 GRCh37 |
1252 | 1459 | |
DIDO1 | - | - |
GRCh38 GRCh37 |
90 | 140 | |
GATA5 | - | - |
GRCh38 GRCh37 |
457 | 488 | |
GID8 | - | - |
GRCh38 GRCh37 |
9 | 57 | |
HAR1A | - | - |
GRCh38 GRCh37 |
- | 57 |
There are 15 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) |
|
Jul 20, 2015 | RCV000207152.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Feb 14, 2024