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Variant : CV435819 (GRCh37/hg19 8p21.3(chr8:21521340-22492009)x4) Homo sapiens

Symbol: CV435819
Name: GRCh37/hg19 8p21.3(chr8:21521340-22492009)x4
Condition: See cases [RCV000510404]
Clinical Significance: uncertain significance
Last Evaluated: 09/22/2014
Review Status: no assertion criteria provided
Related Genes: BIN3   BMP1   C8orf58   CCAR2   DMTN   DOK2   FAM160B2   FGF17   GFRA2   HR   LGI3   MIR320A   NPM2   NUDT18   PDLIM2   PHYHIP   PIWIL2   POLR3D   PPP3CC   REEP4   SFTPC   SLC39A14   SORBS3   XPO7  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37821,521,340 - 22,492,009CLINVAR
Cytogenetic Map88p21.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13443383
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.