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Variant : CV804309 (GRCh37/hg19 20p13(chr20:61568-1305971)x1) Homo sapiens

Symbol: CV804309
Name: GRCh37/hg19 20p13(chr20:61568-1305971)x1
Condition: not provided [RCV001007067]
Clinical Significance: pathogenic
Last Evaluated: 04/11/2019
Review Status: no assertion criteria provided
Related Genes: ANGPT4   C20orf202   C20orf96   CSNK2A1   DEFB125   DEFB126   DEFB127   DEFB128   DEFB129   DEFB132   FAM110A   NRSN2   PSMF1   RAD21L1   RBCK1   RSPO4   SCRT2   SDCBP2   SLC52A3   SNPH   SOX12   SRXN1   TBC1D20   TCF15   TMEM74B   TRIB3   ZCCHC3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372061,568 - 1,305,971CLINVAR
Cytogenetic Map2020p13CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25316811
Created: 2020-04-07
Species: Homo sapiens
Last Modified: 2020-06-30
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.