ClinVar Genomic variation as it relates to human health
GRCh38/hg38 7q11.23(chr7:75769688-76066509)x1
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 | |||
CCL24 | - | - |
GRCh38 GRCh37 |
3 | 42 | |
CCL26 | - | - |
GRCh38 GRCh37 |
10 | 50 | |
LOC121740687 | - | - | - | GRCh38 | - | 14 |
LOC123956166 | - | - | - | GRCh38 | - | 14 |
LOC123956167 | - | - | - | GRCh38 | - | 14 |
LOC123956168 | - | - | - | GRCh38 | - | 14 |
LOC126860075 | - | - | - | GRCh38 | - | 96 |
LOC129998677 | - | - | - | GRCh38 | - | 14 |
LOC129998678 | - | - | - | GRCh38 | - | 14 |
LOC129998679 | - | - | - | GRCh38 | - | 14 |
There are 17 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 |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 12, 2011 | RCV000052686.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024