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Variant : CV605859 (GRCh37/hg19 15q11.2(chr15:20807537-21200585)x1) Homo sapiens

Symbol: CV605859
Name: GRCh37/hg19 15q11.2(chr15:20807537-21200585)x1
Condition: not provided [RCV000751159]
Clinical Significance: benign
Last Evaluated: 10/10/2012
Review Status: no assertion criteria provided
Related Genes: POTEB2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371520,807,537 - 21,200,585CLINVAR
Cytogenetic Map1515q11.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14366485
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.