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Variant : CV605862 (GRCh37/hg19 15q11.2(chr15:20839330-21203038)x3) Homo sapiens

Symbol: CV605862
Name: GRCh37/hg19 15q11.2(chr15:20839330-21203038)x3
Condition: not provided [RCV000751162]
Clinical Significance: benign
Last Evaluated: 05/23/2012
Review Status: no assertion criteria provided
Related Genes: POTEB2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371520,839,330 - 21,203,038CLINVAR
Cytogenetic Map1515q11.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14366488
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-01
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.