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Variant : CV439793 (GRCh37/hg19 20q11.21(chr20:29425357-30226690)x3) Homo sapiens

Symbol: CV439793
Name: GRCh37/hg19 20q11.21(chr20:29425357-30226690)x3
Condition: See cases [RCV000515558]
Clinical Significance: uncertain significance
Last Evaluated: 05/31/2017
Review Status: no assertion criteria provided
Related Genes: COX4I2   DEFB115   DEFB116   DEFB118   DEFB119   DEFB121   DEFB123   DEFB124   HM13   ID1   LINC01597   REM1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372029,425,357 - 30,226,690CLINVAR
Cytogenetic Map2020q11.21CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13463114
Created: 2017-12-12
Species: Homo sapiens
Last Modified: 2020-09-22
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.