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Variant : CV436566 (GRCh37/hg19 11q25(chr11:133609389-134938470)x1) Homo sapiens

Symbol: CV436566
Name: GRCh37/hg19 11q25(chr11:133609389-134938470)x1
Condition: See cases [RCV000512352]
Clinical Significance: uncertain significance
Last Evaluated: 08/01/2014
Review Status: no assertion criteria provided
Related Genes: ACAD8   B3GAT1   GLB1L2   GLB1L3   IGSF9B   JAM3   LINC02714   LINC02743   NCAPD3   SPATA19   THYN1   VPS26B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711133,609,389 - 134,938,470CLINVAR
Cytogenetic Map1111q25CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13445316
Created: 2017-11-07
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.