ClinVar Genomic variation as it relates to human health
GRCh38/hg38 11p15.1(chr11:18526222-20748125)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 | |||
CSRP3 | - | - |
GRCh38 GRCh37 |
420 | 458 | |
CSRP3-AS1 | - | - | - | GRCh38 | - | 87 |
DBX1 | - | - |
GRCh38 GRCh37 |
5 | 30 | |
E2F8 | - | - |
GRCh38 GRCh37 |
- | 78 | |
HTATIP2 | - | - |
GRCh38 GRCh37 |
17 | 32 | |
IGSF22 | - | - | - |
GRCh38 GRCh37 |
6 | 115 |
IGSF22-AS1 | - | - | - | GRCh38 | - | 119 |
LEISA1 | - | - | - | GRCh38 | - | 15 |
LOC110121487 | - | - | - | GRCh38 | - | 4 |
LOC110121488 | - | - | - | GRCh38 | - | 2 |
There are 75 more genes affected by this variant. See the full set of genes in Variation Viewer (GRCh38 , GRCh37 , NCBI36).
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Dec 22, 2010 | RCV000134932.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024