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Variant : CV436041 (GRCh37/hg19 20q11.21(chr20:29833535-30599771)x3) Homo sapiens

Symbol: CV436041
Name: GRCh37/hg19 20q11.21(chr20:29833535-30599771)x3
Condition: See cases [RCV000511585]
Clinical Significance: uncertain significance
Last Evaluated: 07/21/2014
Review Status: no assertion criteria provided
Related Genes: BCL2L1   CCM2L   COX4I2   DEFB115   DEFB116   DEFB118   DEFB119   DEFB121   DEFB123   DEFB124   DUSP15   FOXS1   HM13   ID1   MYLK2   PDRG1   REM1   TPX2   TTLL9   XKR7  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372029,833,535 - 30,599,771CLINVAR
Cytogenetic Map2020q11.21CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13444555
Created: 2017-11-07
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.