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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5704956mobile element insertion1nstd211human GRCh38 chr11: 2,980,157-2,980,157 , GRCh37.p13 chr11: 3,001,387-3,001,387 NAP1L4
    nsv5699172mobile element insertion1nstd211human GRCh38 chr11: 2,990,284-2,990,284 , GRCh37.p13 chr11: 3,011,514-3,011,514 NAP1L4
    nsv5603180copy number variation1nstd207human GRCh38 chr11: 2,981,011-2,983,761 , GRCh37.p13 chr11: 3,002,241-3,004,991 NAP1L4
    nsv5510182copy number variation1nstd206human GRCh38 chr11: 2,977,068-2,977,171 , GRCh37.p13 chr11: 2,998,298-2,998,401 NAP1L4
    nsv5505069copy number variation1nstd206human GRCh38 chr11: 2,980,971-2,983,865 , GRCh37.p13 chr11: 3,002,201-3,005,095 NAP1L4
    nsv5494060copy number variation1nstd206human GRCh38 chr11: 2,977,493-3,015,199 , GRCh37.p13 chr11: 2,998,723-3,036,429 CARS1, NAP1L4
    nsv5407501mobile element insertion1nstd206human GRCh38 chr11: 2,980,157-2,980,208 , GRCh37.p13 chr11: 3,001,387-3,001,438 NAP1L4
    nsv5399267mobile element insertion1nstd206human GRCh38 chr11: 2,990,284-2,990,298 , GRCh37.p13 chr11: 3,011,514-3,011,528 NAP1L4
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5256639copy number variation1nstd204human GRCh38.p13 chr11: 2,988,021-2,990,270 , GRCh37.p13 chr11: 3,009,251-3,011,500 NAP1L4
    nsv5244220copy number variation1nstd204human GRCh38.p13 chr11: 2,981,421-2,984,120 , GRCh37.p13 chr11: 3,002,651-3,005,350 NAP1L4
    nsv4977902copy number variation1nstd200human GRCh38 chr11: 2,967,856-2,968,020 , GRCh37.p13 chr11: 2,989,086-2,989,250 NAP1L4
    nsv4848976copy number variation1nstd200human GRCh37 chr11: 3,002,325-3,005,063 , GRCh38.p12 chr11: 2,981,095-2,983,833 , GRCh38.p12 chr11|NT_187585.1: 212,165-214,911 NAP1L4
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4679705copy number variation1nstd189human GRCh37.p13 chr11: 2,339,823-3,832,257 , GRCh38.p12 chr11: 2,318,593-3,811,027 , ART1, 50 more genes
    nsv4675579copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,683,937-3,207,439 , GRCh38.p12 chr11|NT_187585.1: 1-296,883 , GRCh38.p12 chr11: 2,662,707-3,186,209 CDKN1C, KCNQ1DN, 15 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
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