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Variant : CV382107 (GRCh37/hg19 20q11.21(chr20:29877878-30231917)x3) Homo sapiens

Symbol: CV382107
Name: GRCh37/hg19 20q11.21(chr20:29877878-30231917)x3
Condition: See cases [RCV000448484]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: COX4I2   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
GRCh372029,877,878 - 30,231,917CLINVAR
Cytogenetic Map2020q11.21CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853192
Created: 2017-04-11
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.