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Variant : CV439776 (GRCh37/hg19 11q25(chr11:133923605-134934063)x3) Homo sapiens

Symbol: CV439776
Name: GRCh37/hg19 11q25(chr11:133923605-134934063)x3
Condition: See cases [RCV000515562]
Clinical Significance: uncertain significance
Last Evaluated: 04/27/2017
Review Status: no assertion criteria provided
Related Genes: ACAD8   B3GAT1   GLB1L2   GLB1L3   JAM3   LINC02714   NCAPD3   THYN1   VPS26B  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3711133,923,605 - 134,934,063CLINVAR
Cytogenetic Map1111q25CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 13462285
Created: 2017-12-12
Species: Homo sapiens
Last Modified: 2020-07-28
Status: ACTIVE


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