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Variant : CV803697 (GRCh37/hg19 11q25(chr11:134054327-134200885)x1) Homo sapiens

Symbol: CV803697
Name: GRCh37/hg19 11q25(chr11:134054327-134200885)x1
Condition: not provided [RCV001006465]
Clinical Significance: uncertain significance
Last Evaluated: 08/23/2018
Review Status: no assertion criteria provided
Related Genes: ACAD8   GLB1L3   NCAPD3   THYN1   VPS26B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711134,054,327 - 134,200,885CLINVAR
Cytogenetic Map1111q25CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25316132
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.