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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5722627mobile element insertion2nstd211human GRCh38 chr8: 19,937,357-19,937,357 , GRCh37.p13 chr8: 19,794,868-19,794,868 LPL
    nsv5698478mobile element insertion2nstd211human GRCh38 chr8: 19,956,770-19,956,770 , GRCh37.p13 chr8: 19,814,281-19,814,281 LPL
    nsv5673948copy number variation1nstd102humanPathogenic GRCh37 chr8: 19,810,811-19,811,874 , GRCh38.p12 chr8: 19,953,300-19,954,363 LPL
    nsv5554187mobile element insertion1nstd206human GRCh38 chr8: 19,937,357-19,937,408 , GRCh37.p13 chr8: 19,794,868-19,794,919 LPL
    nsv5481561copy number variation1nstd206human GRCh38 chr8: 19,911,946-20,226,032 , GRCh37.p13 chr8: 19,769,457-20,083,543 , ATP6V1B2, 6 more genes
    nsv5394328mobile element insertion1nstd206human GRCh38 chr8: 19,956,770-19,956,821 , GRCh37.p13 chr8: 19,814,281-19,814,332 LPL
    nsv5379109translocation1nstd200human GRCh38 chr8: 19,951,106-19,951,106 , GRCh38 chr8: 19,950,899-19,950,899 , GRCh37.p13 chr8: 19,808,617-19,808,617 , GRCh37.p13 chr8: 19,808,410-19,808,410 LPL
    nsv5367379translocation1nstd200human GRCh38 chr8: 19,937,357-19,937,357 , GRCh38 chr4: 15,869,741-15,869,741 , GRCh37.p13 chr4: 15,871,364-15,871,364 , GRCh37.p13 chr8: 19,794,868-19,794,868 LPL
    nsv5335429translocation1nstd200human GRCh37 chr8: 19,808,410-19,808,410 , GRCh37 chr8: 19,808,617-19,808,617 , GRCh38.p12 chr8: 19,950,899-19,950,899 , GRCh38.p12 chr8: 19,951,106-19,951,106 LPL
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5192399mobile element insertion1nstd203human GRCh38 chr8: 19,937,344-19,937,355 , GRCh37.p13 chr8: 19,794,855-19,794,866 LPL
    nsv5183382mobile element insertion1nstd203human GRCh38 chr8: 19,937,348-19,937,357 , GRCh37.p13 chr8: 19,794,859-19,794,868 LPL
    nsv5119905mobile element insertion1nstd203human GRCh38 chr8: 19,949,834-19,949,845 , GRCh37.p13 chr8: 19,807,345-19,807,356 LPL
    nsv4959541copy number variation1nstd200human GRCh38 chr8: 19,945,185-19,946,756 , GRCh37.p13 chr8: 19,802,696-19,804,267 LPL
    nsv4959540copy number variation1nstd200human GRCh38 chr8: 19,943,063-19,944,933 , GRCh37.p13 chr8: 19,800,574-19,802,444 LPL
    nsv4954236copy number variation1nstd200human GRCh38 chr8: 19,955,962-19,958,022 , GRCh37.p13 chr8: 19,813,473-19,815,533 LPL
    nsv4954234copy number variation1nstd200human GRCh38 chr8: 19,892,211-20,771,424 , GRCh37.p13 chr8: 19,749,722-20,628,935 , LOC105379312, 15 more genes
    nsv4821404copy number variation1nstd200human GRCh37 chr8: 19,802,696-19,804,267 , GRCh38.p12 chr8: 19,945,185-19,946,756 LPL
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4675699copy number variation1nstd102humanUncertain significance GRCh37 chr8: 19,334,399-19,809,695 , GRCh38.p12 chr8: 19,476,888-19,952,184 LOC105379309, LOC107986920, 4 more genes
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