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Variant : CV436304 (GRCh37/hg19 20q13.2-13.31(chr20:54541125-55162415)x3) Homo sapiens

Symbol: CV436304
Name: GRCh37/hg19 20q13.2-13.31(chr20:54541125-55162415)x3
Condition: See cases [RCV000511263]
Clinical Significance: uncertain significance
Last Evaluated: 08/26/2015
Review Status: no assertion criteria provided
Related Genes: AURKA   CASS4   CBLN4   CSTF1   FAM209A   FAM209B   FAM210B   GCNT7   MC3R   RTF2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372054,541,125 - 55,162,415CLINVAR
Cytogenetic Map2020q13.2-13.31CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444238
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-12-03
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.