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Variant : CV804331 (GRCh37/hg19 20q11.21(chr20:29651839-30195919)x3) Homo sapiens

Symbol: CV804331
Name: GRCh37/hg19 20q11.21(chr20:29651839-30195919)x3
Condition: not provided [RCV001007089]
Clinical Significance: likely benign
Last Evaluated: 01/04/2019
Review Status: no assertion criteria provided
Related Genes: DEFB115   DEFB116   DEFB118   DEFB119   DEFB121   DEFB123   DEFB124   HM13   ID1   REM1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372029,651,839 - 30,195,919CLINVAR
Cytogenetic Map2020q11.21CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25323132
Created: 2020-04-07
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.