ClinVar Genomic variation as it relates to human health
GRCh37/hg19 22q11.21-11.22(chr22:21915095-22603542)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 | |||
TOP3B | No evidence available | No evidence available |
GRCh38 GRCh37 |
84 | 197 | |
CCDC116 | - | - | - |
GRCh38 GRCh37 |
45 | 147 |
MAPK1 | - | - |
GRCh38 GRCh37 |
42 | 149 | |
MIR130B | - | - |
GRCh38 GRCh37 |
- | 101 | |
PPIL2 | - | - |
GRCh38 GRCh37 |
31 | 136 | |
PPM1F | - | - |
GRCh38 GRCh37 |
56 | 169 | |
PPM1F-AS1 | - | - | - |
GRCh38 GRCh37 |
- | 111 |
SDF2L1 | - | - |
GRCh38 GRCh37 |
9 | 115 | |
UBE2L3 | - | - |
GRCh38 GRCh37 |
3 | 116 | |
VPREB1 | - | - |
GRCh38 GRCh37 |
- | 104 |
There are 2 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh37) and ClinGen Dosage Sensitivity Map.
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Apr 10, 2018 | RCV000849651.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 11, 2022