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Variant : CV674337 (GRCh37/hg19 20p11.21(chr20:24232978-25520939)x3) Homo sapiens

Symbol: CV674337
Name: GRCh37/hg19 20p11.21(chr20:24232978-25520939)x3
Condition: not provided [RCV000847453]
Clinical Significance: uncertain significance
Last Evaluated: 06/27/2017
Review Status: no assertion criteria provided
Related Genes: ABHD12   ACSS1   APMAP   CST7   ENTPD6   GINS1   NINL   PYGB   SYNDIG1   VSX1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372024,232,978 - 25,520,939CLINVAR
Cytogenetic Map2020p11.21CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14978171
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-07-07
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.