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Variant : CV675855 (GRCh37/hg19 11q24.2(chr11:126111090-127755537)x3) Homo sapiens

Symbol: CV675855
Name: GRCh37/hg19 11q24.2(chr11:126111090-127755537)x3
Condition: not provided [RCV000848954]
Clinical Significance: uncertain significance
Last Evaluated: 06/14/2018
Review Status: no assertion criteria provided
Related Genes: AP001993.1   DCPS   FAM118B   FOXRED1   KIRREL3   SRPRA   ST3GAL4   TIRAP  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3711126,111,090 - 127,755,537CLINVAR
Cytogenetic Map1111q24.2CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14980485
Created: 2019-10-08
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.