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Variant : CV673149 (GRCh37/hg19 8p21.3(chr8:21077580-22144930)x1) Homo sapiens

Symbol: CV673149
Name: GRCh37/hg19 8p21.3(chr8:21077580-22144930)x1
Condition: not provided [RCV000846265]
Clinical Significance: uncertain significance
Last Evaluated: 05/11/2017
Review Status: no assertion criteria provided
Related Genes: BMP1   DMTN   DOK2   FAM160B2   FGF17   GFRA2   HR   LGI3   MIR320A   NPM2   NUDT18   PHYHIP   PIWIL2   POLR3D   REEP4   SFTPC   XPO7  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37821,077,580 - 22,144,930CLINVAR
Cytogenetic Map88p21.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14976846
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-31
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.