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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094607copy number variation1nstd102humanUncertain significance GRCh37 chr16: 8,829,597-11,683,693 , GRCh38.p12 chr16: 8,735,740-11,589,837 LOC400499, NUBP1, 58 more genes
    nsv7094554copy number variation1nstd102humanPathogenic GRCh37 chr16: 10,637,407-10,971,259 , GRCh38.p12 chr16: 10,543,550-10,877,402 TEKT5, NUBP1, 10 more genes
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv6973888copy number variation1nstd229human GRCh38 chr16: 10,747,891-10,751,723 , GRCh37.p13 chr16: 10,841,748-10,845,580 NUBP1
    nsv6972105copy number variation1nstd229human GRCh38 chr16: 10,729,501-10,742,700 , GRCh37.p13 chr16: 10,823,358-10,836,557 NUBP1
    nsv6967733copy number variation1nstd229human GRCh38 chr16: 10,769,592-10,769,652 , GRCh37.p13 chr16: 10,863,449-10,863,509 NUBP1, TVP23A
    nsv6966826copy number variation1nstd229human GRCh38 chr16: 10,646,382-10,861,820 , GRCh37.p13 chr16: 10,740,239-10,955,677 NUBP1, TEKT5, 8 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6637308copy number variation1nstd102humanUncertain significance GRCh37 chr16: 10,423,631-12,176,517 , GRCh38.p12 chr16: 10,329,774-12,082,660 LOC400499, RSL1D1, 46 more genes
    nsv6623176copy number variation1nstd224human GRCh37 chr16: 10,640,898-10,927,933 , GRCh38.p12 chr16: 10,547,041-10,834,076 EMP2, TVP23A, 8 more genes
    nsv6593922inversion1nstd223human GRCh38 chr16: 10,744,954-10,745,484 , GRCh37.p13 chr16: 10,838,811-10,839,341 NUBP1
    nsv6507343copy number variation1nstd223human GRCh38 chr16: 10,144,159-11,379,723 , GRCh37.p13 chr16: 10,238,016-11,473,580 LINC01290, LOC105371078, 35 more genes
    nsv6500831copy number variation1nstd223human GRCh38 chr16: 10,669,159-11,475,479 , GRCh37.p13 chr16: 10,763,016-11,569,335 MTCYBP33, MTND4LP24, 27 more genes
    nsv6309886copy number variation2nstd102humanUncertain significance GRCh37 chr16: 8,829,597-11,650,586 , GRCh38.p12 chr16: 8,735,740-11,556,730 NUBP1, TVP23A, 58 more genes
    nsv6274715copy number variation1nstd214human GRCh38 chr16: 10,764,778-10,764,847 , GRCh37.p13 chr16: 10,858,635-10,858,704 TVP23A, NUBP1
    nsv6272027copy number variation1nstd214human GRCh38 chr16: 10,763,926-10,764,069 , GRCh37.p13 chr16: 10,857,783-10,857,926 TVP23A, NUBP1
    nsv6271750copy number variation1nstd214human GRCh38 chr16: 10,769,590-10,769,651 , GRCh37.p13 chr16: 10,863,447-10,863,508 NUBP1, TVP23A
    nsv6271729copy number variation1nstd214human GRCh38 chr16: 10,764,742-10,764,847 , GRCh37.p13 chr16: 10,858,599-10,858,704 TVP23A, NUBP1
    nsv6227616insertion1nstd214human GRCh38 chr16: 10,762,833-10,762,833 , GRCh37.p13 chr16: 10,856,690-10,856,690 NUBP1, TVP23A
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
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