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Variant : CV437111 (GRCh37/hg19 11q25(chr11:133328654-134177275)x3) Homo sapiens

Symbol: CV437111
Name: GRCh37/hg19 11q25(chr11:133328654-134177275)x3
Condition: See cases [RCV000510975]
Clinical Significance: likely benign
Last Evaluated: 07/15/2015
Review Status: no assertion criteria provided
Related Genes: ACAD8   GLB1L3   IGSF9B   JAM3   LINC02743   NCAPD3   OPCML   SPATA19   THYN1   VPS26B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711133,328,654 - 134,177,275CLINVAR
Cytogenetic Map1111q25CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13443952
Created: 2017-11-07
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.