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Variant : CV248425 (GRCh37/hg19 8q24.3(chr8:143762893-143867731)x3) Homo sapiens

Symbol: CV248425
Name: GRCh37/hg19 8q24.3(chr8:143762893-143867731)x3
Condition: See cases [RCV000239918]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: LY6D   LY6K   LYNX1   LYPD2   PSCA   SLURP1   THEM6  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh378143,762,893 - 143,867,731CLINVAR
Cytogenetic Map88q24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11541403
Created: 2016-10-11
Species: Homo sapiens
Last Modified: 2020-03-17
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.