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Variant : CV803696 (GRCh37/hg19 11q25(chr11:133841587-134507651)x3) Homo sapiens

Symbol: CV803696
Name: GRCh37/hg19 11q25(chr11:133841587-134507651)x3
Condition: not provided [RCV001006464]
Clinical Significance: uncertain significance
Last Evaluated: 12/12/2018
Review Status: no assertion criteria provided
Related Genes: ACAD8   B3GAT1   GLB1L2   GLB1L3   JAM3   NCAPD3   THYN1   VPS26B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711133,841,587 - 134,507,651CLINVAR
Cytogenetic Map1111q25CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25322041
Created: 2020-04-07
Species: Homo sapiens
Last Modified: 2020-07-28
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.