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Variant : CV382665 (GRCh37/hg19 11q14.1-14.2(chr11:85324893-85757693)x1) Homo sapiens

Symbol: CV382665
Name: GRCh37/hg19 11q14.1-14.2(chr11:85324893-85757693)x1
Condition: See cases [RCV000448261]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: CCDC83   CCDC89   CREBZF   DLG2   PICALM   SYTL2   TMEM126A   TMEM126B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371185,324,893 - 85,757,693CLINVAR
Cytogenetic Map1111q14.1-14.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12852971
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-03-24
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.