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Variant : CV604924 (GRCh37/hg19 11q24.2(chr11:125818237-126315727)x3) Homo sapiens

Symbol: CV604924
Name: GRCh37/hg19 11q24.2(chr11:125818237-126315727)x3
Condition: not provided [RCV000750224]
Clinical Significance: benign
Last Evaluated: 11/04/2016
Review Status: no assertion criteria provided
Related Genes: CDON   DCPS   FAM118B   FOXRED1   KIRREL3   RPUSD4   SRPRA   ST3GAL4   TIRAP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711125,818,237 - 126,315,727CLINVAR
Cytogenetic Map1111q24.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14365552
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-08-04
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.