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Variant : CV216098 (GRCh37/hg19 20p12.1(chr20:16730002-17286002)x3) Homo sapiens

Symbol: CV216098
Name: GRCh37/hg19 20p12.1(chr20:16730002-17286002)x3
Condition: See cases [RCV000203444]
Clinical Significance: uncertain significance
Last Evaluated: 11/02/2015
Review Status: criteria provided, single submitter
Related Genes: OTOR   PCSK2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372016,730,002 - 17,286,002CLINVAR
Cytogenetic Map2020p12.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 10766521
Created: 2016-02-09
Species: Homo sapiens
Last Modified: 2020-06-23
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.