ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q26.13-26.2(chr10:126652011-128433378)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 | |||
ADAM12 | - | - |
GRCh38 GRCh37 |
55 | 128 | |
BCCIP | - | - |
GRCh38 GRCh37 |
13 | 274 | |
C10orf90 | - | - |
GRCh38 GRCh37 |
14 | 87 | |
CTBP2 | - | - |
GRCh38 GRCh37 |
56 | 122 | |
DHX32 | - | - |
GRCh38 GRCh37 |
159 | 421 | |
EDRF1 | - | - | - |
GRCh38 GRCh37 |
38 | 112 |
FANK1 | - | - |
GRCh38 GRCh37 |
21 | 91 | |
MMP21 | - | - |
GRCh38 GRCh37 |
98 | 166 | |
TEX36 | - | - | - |
GRCh38 GRCh37 |
6 | 78 |
UROS | - | - |
GRCh38 GRCh37 |
129 | 197 |
There is 1 more gene 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) |
|
Jan 8, 2018 | RCV000683267.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Apr 25, 2022