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Variant : CV803689 (GRCh37/hg19 11q24.2(chr11:126201307-126466438)x3) Homo sapiens

Symbol: CV803689
Name: GRCh37/hg19 11q24.2(chr11:126201307-126466438)x3
Condition: not provided [RCV001006457]
Clinical Significance: uncertain significance
Last Evaluated: 09/20/2018
Review Status: no assertion criteria provided
Related Genes: DCPS   KIRREL3   ST3GAL4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711126,201,307 - 126,466,438CLINVAR
Cytogenetic Map1111q24.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25322006
Created: 2020-04-07
Species: Homo sapiens
Last Modified: 2020-07-28
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.