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Variant : CV555056 (GRCh37/hg19 11q25(chr11:132187876-134938470)x1) Homo sapiens

Symbol: CV555056
Name: GRCh37/hg19 11q25(chr11:132187876-134938470)x1
Condition: not provided [RCV000683361]
Clinical Significance: pathogenic
Last Evaluated: 07/17/2017
Review Status: no assertion criteria provided
Related Genes: ACAD8   B3GAT1   GLB1L2   GLB1L3   IGSF9B   JAM3   LINC02714   LINC02743   NCAPD3   NTM   OPCML   SPATA19   THYN1   VPS26B  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3711132,187,876 - 134,938,470CLINVAR
Cytogenetic Map1111q25CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 13796506
Created: 2018-10-09
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.