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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5712254mobile element insertion2nstd211human GRCh38 chr16: 66,746,170-66,746,170 , GRCh37.p13 chr16: 66,780,073-66,780,073 DYNC1LI2
    nsv5561052sequence alteration1nstd206human GRCh38 chr16: 66,734,974-66,735,638 , GRCh37.p13 chr16: 66,768,877-66,769,541 DYNC1LI2
    nsv5556229inversion1nstd206human GRCh38 chr16: 66,734,951-66,735,660 , GRCh37.p13 chr16: 66,768,854-66,769,563 DYNC1LI2
    nsv5428704mobile element insertion1nstd206human GRCh38 chr16: 66,746,170-66,746,221 , GRCh37.p13 chr16: 66,780,073-66,780,124 DYNC1LI2
    nsv5380484translocation1nstd200human GRCh38 chr16: 66,751,150-66,751,150 , GRCh38 chr2: 85,215,067-85,215,067 , GRCh37.p13 chr16: 66,785,053-66,785,053 , GRCh37.p13 chr2: 85,442,190-85,442,190 DYNC1LI2, TCF7L1, 2 more genes
    nsv5380483translocation1nstd200human GRCh38 chr16: 66,751,588-66,751,588 , GRCh38 chr2: 85,215,066-85,215,066 , GRCh37.p13 chr16: 66,785,491-66,785,491 , GRCh37.p13 chr2: 85,442,189-85,442,189 DYNC1LI2, TCF7L1, 2 more genes
    nsv5363296translocation1nstd200human GRCh38 chr16: 66,746,563-66,746,563 , GRCh38 chr6: 108,956,793-108,956,793 , GRCh37.p13 chr16: 66,780,466-66,780,466 , GRCh37.p13 chr6: 109,277,996-109,277,996 ARMC2, DYNC1LI2
    nsv5363295translocation1nstd200human GRCh38 chr16: 66,748,028-66,748,028 , GRCh38 chr6: 108,956,792-108,956,792 , GRCh37.p13 chr16: 66,781,931-66,781,931 , GRCh37.p13 chr6: 109,277,995-109,277,995 DYNC1LI2, ARMC2
    nsv5202690mobile element deletion1nstd204human GRCh38.p13 chr16: 66,724,930-66,725,230 , GRCh37.p13 chr16: 66,758,833-66,759,133 DYNC1LI2
    nsv5159084mobile element insertion1nstd203human GRCh38 chr16: 66,746,155-66,746,170 , GRCh37.p13 chr16: 66,780,058-66,780,073 DYNC1LI2
    nsv5141970mobile element insertion1nstd203human GRCh38 chr16: 66,747,911-66,747,927 , GRCh37.p13 chr16: 66,781,814-66,781,830 DYNC1LI2
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4786098mobile element deletion1nstd200human GRCh37 chr16: 66,758,843-66,759,124 , GRCh38.p12 chr16: 66,724,940-66,725,221 DYNC1LI2
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4675201copy number variation1nstd102humanPathogenic GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280 LOC100420066, LINC00920, 143 more genes
    nsv4578635copy number variation1nstd102humanUncertain significance GRCh37 chr16: 64,981,506-66,806,661 , GRCh38.p12 chr16: 64,947,603-66,772,758 CKLF-CMTM1, BEAN1, 21 more genes
    nsv4576419mobile element insertion1nstd166human GRCh37.p13 chr16: 66,775,537-66,775,537 , GRCh38.p12 chr16: 66,741,634-66,741,634 DYNC1LI2
    nsv4501963mobile element insertion1nstd166human GRCh37.p13 chr16: 66,780,058-66,780,058 , GRCh38.p12 chr16: 66,746,155-66,746,155 DYNC1LI2
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