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Variant : CV156716 (GRCh38/hg38 15q14(chr15:34402995-34549216)x1) Homo sapiens

Symbol: CV156716
Name: GRCh38/hg38 15q14(chr15:34402995-34549216)x1
Condition: See cases [RCV000136186]
Clinical Significance: benign
Last Evaluated: 02/06/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GOLGA8A   GOLGA8B   MIR1233-2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_34402995)_(34549216_?)del
NC_000015.9:g.(?_34695196)_(34841417_?)del
NC_000015.8:g.(?_32482488)_(32628709_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381534,402,995 - 34,549,216CLINVAR
GRCh371534,695,196 - 34,841,417CLINVAR
Build 361532,482,488 - 32,628,709CLINVAR
Cytogenetic Map1515q14CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483747
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.