ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p13-12(chr11:32782607-36404823)
Germline
Classification
(1)
Uncertain significance
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 | |||
ABTB2 | - | - | - |
GRCh38 GRCh37 |
75 | 99 |
APIP | - | - |
GRCh38 GRCh37 |
11 | 47 | |
C11orf91 | - | - | - |
GRCh38 GRCh37 |
3 | 24 |
CAPRIN1 | - | - |
GRCh38 GRCh37 |
44 | 63 | |
CAT | - | - |
GRCh38 GRCh37 |
40 | 63 | |
CD44 | - | - |
GRCh38 GRCh37 |
60 | 92 | |
CD59 | - | - |
GRCh38 GRCh37 |
94 | 115 | |
COMMD9 | - | - |
GRCh38 GRCh37 |
13 | 32 | |
CSTF3 | - | - |
GRCh38 GRCh37 |
15 | 44 | |
DEPDC7 | - | - |
GRCh38 GRCh37 |
14 | 43 |
There are 18 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) |
|
Mar 1, 2022 | RCV002052921.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 16, 2022