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Variant : CV604937 (GRCh37/hg19 11q25(chr11:131740926-134934063)x1) Homo sapiens

Symbol: CV604937
Name: GRCh37/hg19 11q25(chr11:131740926-134934063)x1
Condition: not provided [RCV000750237]
Clinical Significance: pathogenic
Last Evaluated: 04/24/2015
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)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711131,740,926 - 134,934,063CLINVAR
Cytogenetic Map1111q25CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14365565
Created: 2019-02-12
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.