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Variant : CV593327 (GRCh37/hg19 15q11.1-11.2(chr15:20212798-22652330)x1) Homo sapiens

Symbol: CV593327
Name: GRCh37/hg19 15q11.1-11.2(chr15:20212798-22652330)x1
Condition: not provided [RCV000738627]
Clinical Significance: benign
Last Evaluated: 08/20/2016
Review Status: no assertion criteria provided
Related Genes: GOLGA6L6   OR4M2   OR4N4   POTEB   POTEB2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371520,212,798 - 22,652,330CLINVAR
Cytogenetic Map1515q11.1-11.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14354007
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-08
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.