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Variant : CV161382 (GRCh38/hg38 5p15.33(chr5:314795-496067)x1) Homo sapiens

Symbol: CV161382
Name: GRCh38/hg38 5p15.33(chr5:314795-496067)x1
Condition: See cases [RCV000140335]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AHRR   EXOC3   EXOC3-AS1   PDCD6   SLC9A3   SLC9A3-AS1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000005.10:g.(?_314795)_(496067_?)del
NC_000005.9:g.(?_314910)_(496182_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh385314,795 - 496,067CLINVAR
GRCh375314,910 - 496,182CLINVAR
Build 365367,910 - 549,182CLINVAR
Cytogenetic Map55p15.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487865
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.