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Variant : CV436405 (GRCh37/hg19 20p13(chr20:61568-2824960)x3) Homo sapiens

Symbol: CV436405
Name: GRCh37/hg19 20p13(chr20:61568-2824960)x3
Condition: See cases [RCV000511991]
Clinical Significance: uncertain significance
Last Evaluated: 07/06/2015
Review Status: no assertion criteria provided
Related Genes: ANGPT4   C20orf141   C20orf202   C20orf96   CPXM1   CSNK2A1   DEFB125   DEFB126   DEFB127   DEFB128   DEFB129   DEFB132   EBF4   FAM110A   FKBP1A   IDH3B   MIR1292   NOP56   NRSN2   NSFL1C   PCED1A   PDYN   PSMF1   RAD21L1   RBCK1   RSPO4   SCRT2   SDCBP2   SIRPA   SIRPB1   SIRPB2   SIRPD   SIRPG   SLC52A3   SNPH   SNRPB   SOX12   SRXN1   STK35   TBC1D20   TCF15   TGM3   TGM6   TMC2   TMEM239   TMEM74B   TRIB3   VPS16   ZCCHC3   ZNF343  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372061,568 - 2,824,960CLINVAR
Cytogenetic Map2020p13CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13444960
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-24
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.