ClinVar Genomic variation as it relates to human health
GRCh38/hg38 5q35.3(chr5:180636182-181269805)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 | |||
BTNL3 | - | - |
GRCh38 GRCh37 |
37 | 71 | |
BTNL8 | - | - |
GRCh38 GRCh37 |
19 | 65 | |
BTNL9 | - | - |
GRCh38 GRCh37 |
64 | 99 | |
CTC-338M12.4 | - | - | - | GRCh38 | - | 12 |
FLT4 | - | - |
GRCh38 GRCh37 |
380 | 460 | |
HEIH | - | - | GRCh38 | - | 12 | |
LINC00847 | - | - | - | GRCh38 | - | 12 |
LINC01962 | - | - | - | GRCh38 | - | 10 |
LINC02222 | - | - | - | GRCh38 | - | 12 |
LOC123575638 | - | - | - | GRCh38 | - | 12 |
There are 82 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 |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Dec 22, 2010 | RCV000136903.5 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024