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Variant : CV595867 (GRCh37/hg19 20q11.21(chr20:29929692-30070239)x3) Homo sapiens

Symbol: CV595867
Name: GRCh37/hg19 20q11.21(chr20:29929692-30070239)x3
Condition: not provided [RCV000741167]
Clinical Significance: benign
Last Evaluated: 09/15/2015
Review Status: no assertion criteria provided
Related Genes: DEFB118   DEFB119   DEFB121   DEFB123   DEFB124   REM1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372029,929,692 - 30,070,239CLINVAR
Cytogenetic Map2020q11.21CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14356541
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-09-08
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.