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Variant : CV437236 (GRCh37/hg19 20p13(chr20:381794-1268103)x3) Homo sapiens

Symbol: CV437236
Name: GRCh37/hg19 20p13(chr20:381794-1268103)x3
Condition: See cases [RCV000510434]
Clinical Significance: uncertain significance
Last Evaluated: 08/15/2014
Review Status: no assertion criteria provided
Related Genes: ANGPT4   C20orf202   CSNK2A1   FAM110A   PSMF1   RAD21L1   RBCK1   RSPO4   SCRT2   SLC52A3   SNPH   SRXN1   TBC1D20   TCF15   TMEM74B  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3720381,794 - 1,268,103CLINVAR
Cytogenetic Map2020p13CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13443413
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-06-23
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.