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Variant : CV595803 (GRCh37/hg19 20p12.2(chr20:10384819-10650354)x3) Homo sapiens

Symbol: CV595803
Name: GRCh37/hg19 20p12.2(chr20:10384819-10650354)x3
Condition: not provided [RCV000741103]
Clinical Significance: benign
Last Evaluated: 04/09/2013
Review Status: no assertion criteria provided
Related Genes: JAG1   MKKS   SLX4IP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372010,384,819 - 10,650,354CLINVAR
Cytogenetic Map2020p12.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14356477
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-31
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.