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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5928392copy number variation1nstd209human GRCh38 chr15: 65,581,273-65,581,440 , GRCh37.p13 chr15: 65,873,611-65,873,778 INTS14
    nsv5585766copy number variation1nstd207human GRCh38 chr15: 65,581,273-65,581,440 , GRCh37.p13 chr15: 65,873,611-65,873,778 INTS14
    nsv5390199copy number variation1nstd186human GRCh37 chr15: 65,873,587-65,873,784 , GRCh38.p12 chr15: 65,581,249-65,581,446 INTS14
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5150933mobile element insertion1nstd203human GRCh38 chr15: 65,581,414-65,581,441 , GRCh37.p13 chr15: 65,873,752-65,873,779 INTS14
    nsv5005513copy number variation1nstd200human GRCh38 chr15: 65,603,688-65,604,612 , GRCh37.p13 chr15: 65,896,026-65,896,950 INTS14
    nsv4849876copy number variation1nstd200human GRCh37 chr15: 65,873,586-65,873,785 , GRCh38.p12 chr15: 65,581,248-65,581,447 INTS14
    nsv4741233copy number variation1nstd199human GRCh37 chr15: 65,873,621-65,873,788 , GRCh38.p12 chr15: 65,581,283-65,581,450 INTS14
    nsv4530555copy number variation1nstd166human GRCh37.p13 chr15: 65,873,999-65,908,000 , GRCh38.p12 chr15: 65,581,661-65,615,662 SLC24A1, INTS14
    nsv4422694copy number variation1nstd174human GRCh37 chr15: 65,873,611-65,873,799 , GRCh38.p12 chr15: 65,581,273-65,581,461 INTS14
    nsv4245235copy number variation1nstd166human GRCh37.p13 chr15: 65,869,870-65,869,935 , GRCh38.p12 chr15: 65,577,532-65,577,597 INTS14, HACD3
    nsv4238450copy number variation1nstd166human GRCh37.p13 chr15: 65,896,101-65,896,885 , GRCh38.p12 chr15: 65,603,763-65,604,547 INTS14
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 MIR4513, LOC727751, 1754 more genes
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