ClinVar Genomic variation as it relates to human health
GRCh37/hg19 11p13(chr11:32573618-34130228)x1
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 | |||
C11orf91 | - | - | - |
GRCh38 GRCh37 |
3 | 24 |
CAPRIN1 | - | - |
GRCh38 GRCh37 |
44 | 63 | |
CCDC73 | - | - |
GRCh38 GRCh37 |
55 | 79 | |
CD59 | - | - |
GRCh38 GRCh37 |
94 | 115 | |
CSTF3 | - | - |
GRCh38 GRCh37 |
15 | 44 | |
DEPDC7 | - | - |
GRCh38 GRCh37 |
14 | 43 | |
EIF3M | - | - |
GRCh38 GRCh37 |
7 | 30 | |
FBXO3 | - | - |
GRCh38 GRCh37 |
17 | 38 | |
HIPK3 | - | - |
GRCh38 GRCh37 |
50 | 78 | |
KIAA1549L | - | - |
GRCh38 GRCh37 |
103 | 131 |
There are 6 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) |
|
Aug 24, 2017 | RCV000683359.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022