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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973864inversion1nstd209human GRCh38 chr20: 29,104,721-29,868,830 , GRCh37.p13 chr9: 66,459,367-68,422,752 FRG2EP, AGGF1P10, 18 more genes
    nsv5966877copy number variation1nstd209human GRCh38 chr20: 29,125,619-30,424,446 , GRCh37.p13 chr20: 25,864,401-29,615,130 DUX4L33, LOC105379476, 27 more genes
    nsv5965062copy number variation1nstd209human GRCh38 chr20: 29,285,033-30,468,916 , GRCh37.p13 chr4: 190,198,664-190,843,361 , GRCh37.p13 chr20: 25,864,401-29,615,130 LOC110467538, RNA5SP532, 27 more genes
    nsv5958416copy number variation1nstd209human GRCh38 chr20: 29,350,778-29,788,349 , GRCh37.p13 chr: NaN-NaN RARRES2P11, FRG1EP, 12 more genes
    nsv5958242copy number variation1nstd209human GRCh38 chr20: 29,300,713-29,742,883 , GRCh37.p13 chr: NaN-NaN DUX4L33, DUX4L34, 14 more genes
    nsv5956670copy number variation1nstd209human GRCh38 chr20: 29,327,704-29,764,880 , GRCh37.p13 chr: NaN-NaN FAM242B, DUX4L36, 12 more genes
    nsv5955838copy number variation1nstd209human GRCh38 chr20: 25,923,975-30,219,168 , GRCh37.p13 chr20: 25,904,611-29,453,844 CDC27P3, LOC105379477, 30 more genes
    nsv5954916copy number variation1nstd209human GRCh38 chr20: 29,108,114-30,407,063 , GRCh37.p13 chr20: 25,864,401-29,615,130 , GRCh37.p13 chr9: 66,459,367-68,422,752 LOC110467522, LOC105379476, 27 more genes
    nsv5952980copy number variation1nstd209human GRCh38 chr20: 28,864,857-29,847,494 , GRCh37.p13 chr20: 25,864,401-29,615,130 , GRCh37.p13 chr9: 66,459,367-68,486,942 FRG2EP, LOC110467522, 19 more genes
    nsv5948031copy number variation1nstd209human GRCh38 chr20: 29,361,988-29,799,580 , GRCh37.p13 chr: NaN-NaN LOC105379477, RARRES2P11, 12 more genes
    nsv5885502copy number variation1nstd209human GRCh38 chr20: 29,523,785-29,558,579 , GRCh37.p13 chrUn|NT_167213.1: 48,684-135,000 , GRCh37.p13 chr20: 29,560,384-29,581,832 FAM242B
    nsv5876095copy number variation1nstd209human GRCh38 chr20: 29,544,203-29,566,313 , GRCh37.p13 chr20: 29,555,991-29,574,899 FAM242B
    nsv5711367mobile element insertion2nstd211human GRCh38 chr20: 29,550,453-29,550,453 , GRCh37.p13 chr20: 29,568,635-29,568,635 FAM242B
    nsv5542588insertion1nstd206human GRCh38 chr20: 29,550,436-29,550,436 , GRCh37.p13 chr20: 29,568,652-29,568,652 FAM242B
    nsv5366053translocation1nstd200human GRCh38 chr20: 30,327,766-30,327,766 , GRCh38 chr20: 29,556,146-29,556,146 , GRCh37.p13 chr20: 29,562,814-29,562,814 , GRCh37.p13 chr20: 29,562,442-29,562,442 FAM242B
    nsv5294768copy number variation1nstd204human GRCh38.p13 chr20: 29,548,801-29,551,000 , GRCh37.p13 chr20: 29,568,089-29,570,281 FAM242B
    nsv5291704copy number variation1nstd204human GRCh38.p13 chr20: 29,551,901-29,569,100 , GRCh37.p13 chr20: 29,555,991-29,567,188 FAM242B
    nsv5289578copy number variation1nstd204human GRCh38.p13 chr20: 29,521,596-29,574,949 , GRCh37.p13 chrUn|NT_167213.1: 48,684-135,000 FAM242B
    nsv5172703mobile element insertion1nstd203human GRCh38 chr20: 29,550,436-29,550,453 , GRCh37.p13 chr20: 29,568,635-29,568,652 FAM242B
    nsv5167911mobile element insertion1nstd203human GRCh38 chr20: 29,550,440-29,550,453 , GRCh37.p13 chr20: 29,568,635-29,568,648 FAM242B
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