ClinVar Genomic variation as it relates to human health
GRCh37/hg19 22q11.21-11.23(chr22:21465661-23666232)x3
Germline
Classification
(1)
Pathogenic
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 | |||
BCR | No evidence available | No evidence available |
GRCh38 GRCh37 |
126 | 294 | |
TOP3B | No evidence available | No evidence available |
GRCh38 GRCh37 |
92 | 205 | |
CCDC116 | - | - | - |
GRCh38 GRCh37 |
54 | 156 |
GGT2 | - | - |
GRCh38 GRCh37 |
9 | 148 | |
GGTLC2 | - | - |
GRCh38 GRCh37 |
- | 126 | |
GNAZ | - | - |
GRCh38 GRCh37 |
- | 135 | |
HIC2 | - | - |
GRCh38 GRCh37 |
52 | 189 | |
IGLC1 | - | - |
GRCh38 GRCh37 |
- | 136 | |
IGLL5 | - | - | - |
GRCh38 GRCh37 |
- | 144 |
MAPK1 | - | - |
GRCh38 GRCh37 |
48 | 155 |
There are 17 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 |
---|---|---|---|---|
Pathogenic (1) |
|
May 10, 2022 | RCV001007496.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 26, 2023