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Variant : CV593528 (GRCh37/hg19 15q24.3(chr15:77586575-77589720)x1) Homo sapiens

Symbol: CV593528
Name: GRCh37/hg19 15q24.3(chr15:77586575-77589720)x1
Condition: not provided [RCV000738828]
Clinical Significance: benign
Last Evaluated: 04/13/2011
Review Status: no assertion criteria provided
Related Genes: PEAK1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371577,586,575 - 77,589,720CLINVAR
Cytogenetic Map1515q24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14354208
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-08-06
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.