ClinVar Genomic variation as it relates to human health
inv(22)(q12.2q12.2)
Germline
Classification
(1)
Likely pathogenic
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 | |||
NF2 | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
2079 | 2127 | |
SEC14L4 | Dosage sensitivity unlikely | No evidence available |
GRCh38 GRCh37 |
27 | 51 | |
AP1B1 | - | - |
GRCh38 GRCh37 |
93 | 124 | |
ASCC2 | - | - |
GRCh38 GRCh37 |
53 | 79 | |
CABP7 | - | - |
GRCh38 GRCh37 |
14 | 43 | |
CASTOR1 | - | - |
GRCh38 GRCh37 |
19 | 41 | |
CCDC157 | - | - |
GRCh38 GRCh37 |
11 | 92 | |
DUSP18 | - | - |
GRCh38 GRCh37 |
- | 42 | |
EWSR1 | - | - |
GRCh38 GRCh37 |
61 | 93 | |
GAL3ST1 | - | - |
GRCh38 GRCh37 |
19 | 43 |
There are 34 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 |
---|---|---|---|---|
Likely pathogenic (1) |
|
May 21, 2019 | RCV000785873.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 15, 2023