ClinVar Genomic variation as it relates to human health
GRCh37/hg19 3p23-22.3(chr3:31859973-33127072)
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 | |||
CCR4 | - | - |
GRCh38 GRCh37 |
18 | 35 | |
CMTM6 | - | - |
GRCh38 GRCh37 |
3 | 26 | |
CMTM7 | - | - |
GRCh38 GRCh37 |
13 | 31 | |
CMTM8 | - | - |
GRCh38 GRCh37 |
13 | 33 | |
CNOT10 | - | - | - |
GRCh38 GRCh38 GRCh37 |
33 | 56 |
DYNC1LI1 | - | - |
GRCh38 GRCh37 |
22 | 39 | |
GLB1 | - | - |
GRCh38 GRCh37 |
1048 | 1161 | |
GPD1L | - | - |
GRCh38 GRCh37 |
362 | 400 | |
OSBPL10 | - | - |
GRCh38 GRCh37 |
50 | 113 | |
TRIM71 | - | - |
GRCh38 GRCh38 GRCh37 |
78 | 95 |
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) |
|
Mar 1, 2022 | RCV002053337.3 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 16, 2022