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Variant : CV161687 (GRCh38/hg38 15q24.2(chr15:75270060-75296694)x3) Homo sapiens

Symbol: CV161687
Name: GRCh38/hg38 15q24.2(chr15:75270060-75296694)x3
Condition: See cases [RCV000140621]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GOLGA6C   GOLGA6D  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_75270060)_(75296694_?)dup
NC_000015.9:g.(?_75562401)_(75589035_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381575,270,060 - 75,296,694CLINVAR
GRCh371575,562,401 - 75,589,035CLINVAR
Build 361573,349,454 - 73,376,088CLINVAR
Cytogenetic Map1515q24.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488151
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.