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Variant : CV672997 (GRCh37/hg19 8p21.3(chr8:21717395-22395625)x3) Homo sapiens

Symbol: CV672997
Name: GRCh37/hg19 8p21.3(chr8:21717395-22395625)x3
Condition: not provided [RCV000846113]
Clinical Significance: uncertain significance
Last Evaluated: 09/26/2017
Review Status: no assertion criteria provided
Related Genes: BMP1   DMTN   DOK2   FAM160B2   FGF17   HR   LGI3   MIR320A   NPM2   NUDT18   PHYHIP   PIWIL2   POLR3D   PPP3CC   REEP4   SFTPC   SLC39A14   XPO7  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37821,717,395 - 22,395,625CLINVAR
Cytogenetic Map88p21.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14976673
Created: 2019-10-08
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.