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Variant : CV675587 (GRCh37/hg19 11q25(chr11:130969272-134938470)x1) Homo sapiens

Symbol: CV675587
Name: GRCh37/hg19 11q25(chr11:130969272-134938470)x1
Condition: not provided [RCV000848686]
Clinical Significance: pathogenic
Last Evaluated: 10/04/2017
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)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711130,969,272 - 134,938,470CLINVAR
Cytogenetic Map1111q25CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14980230
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-08-04
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.