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Variant : CV383378 (GRCh37/hg19 11q24.2(chr11:126183794-126406741)x3) Homo sapiens

Symbol: CV383378
Name: GRCh37/hg19 11q24.2(chr11:126183794-126406741)x3
Condition: See cases [RCV000448471]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: DCPS   KIRREL3   ST3GAL4  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3711126,183,794 - 126,406,741CLINVAR
Cytogenetic Map1111q24.2CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 12853179
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-08-04
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.