ClinVar Genomic variation as it relates to human health
GRCh37/hg19 10q26.13-26.3(chr10:126662496-133985966)x3
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 | |||
ADAM12 | - | - |
GRCh38 GRCh37 |
55 | 128 | |
BCCIP | - | - |
GRCh38 GRCh37 |
13 | 274 | |
BNIP3 | - | - |
GRCh38 GRCh37 |
4 | 115 | |
C10orf90 | - | - |
GRCh38 GRCh37 |
14 | 87 | |
CLRN3 | - | - | - |
GRCh38 GRCh37 |
20 | 107 |
CTBP2 | - | - |
GRCh38 GRCh37 |
54 | 120 | |
DHX32 | - | - |
GRCh38 GRCh37 |
159 | 421 | |
DOCK1 | - | - |
GRCh38 GRCh37 |
99 | 243 | |
EBF3 | - | - |
GRCh38 GRCh37 |
222 | 324 | |
EDRF1 | - | - | - |
GRCh38 GRCh37 |
38 | 112 |
There are 16 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) |
|
Jun 17, 2021 | RCV002474692.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Dec 31, 2022