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Variant : CV673414 (GRCh37/hg19 20p13(chr20:61568-491171)x1) Homo sapiens

Symbol: CV673414
Name: GRCh37/hg19 20p13(chr20:61568-491171)x1
Condition: not provided [RCV000846530]
Clinical Significance: uncertain significance
Last Evaluated: 03/08/2018
Review Status: no assertion criteria provided
Related Genes: C20orf96   CSNK2A1   DEFB125   DEFB126   DEFB127   DEFB128   DEFB129   DEFB132   NRSN2   RBCK1   SOX12   TBC1D20   TRIB3   ZCCHC3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372061,568 - 491,171CLINVAR
Cytogenetic Map2020p13CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977095
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-14
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.