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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116020mobile element insertion1nstd186human GRCh37 chr18: 44,641,894-44,641,945 , GRCh38.p12 chr18: 47,115,523-47,115,574 HDHD2
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5971400insertion1nstd209human GRCh38 chr18: 47,115,505-47,115,505 , GRCh37.p13 chr18: 44,641,876-44,641,876 HDHD2
    nsv5970228inversion1nstd209human GRCh38 chr18: 42,666,448-47,133,105 , GRCh37.p13 chr18: 40,246,413-44,659,476 , ATP5F1A, 50 more genes
    nsv5726778mobile element insertion1nstd211human GRCh38 chr18: 47,108,196-47,108,196 , GRCh37.p13 chr18: 44,634,567-44,634,567 HDHD2
    nsv5718422mobile element insertion1nstd211human GRCh38 chr18: 47,119,323-47,119,323 , GRCh37.p13 chr18: 44,645,694-44,645,694 HDHD2
    nsv5711552mobile element insertion2nstd211human GRCh38 chr18: 47,115,523-47,115,523 , GRCh37.p13 chr18: 44,641,894-44,641,894 HDHD2
    nsv5560621mobile element insertion1nstd206human GRCh38 chr18: 47,108,196-47,108,247 , GRCh37.p13 chr18: 44,634,567-44,634,618 HDHD2
    nsv5555886sequence alteration1nstd206human GRCh37.p13 chr18: 44,617,345-44,857,797 , GRCh38 chr18: 47,090,974-47,331,426 IER3IP1, KATNAL2, 6 more genes
    nsv5530408copy number variation1nstd206human GRCh38 chr18: 47,120,647-47,120,996 , GRCh37.p13 chr18: 44,647,018-44,647,367 HDHD2
    nsv5415918mobile element insertion1nstd206human GRCh38 chr18: 47,115,523-47,115,574 , GRCh37.p13 chr18: 44,641,894-44,641,945 HDHD2
    nsv5381046copy number variation2nstd102humanUncertain significance GRCh37 chr18: 42,281,312-45,423,127 , GRCh38.p12 chr18: 44,701,347-47,896,756 HDHD2, RNU6-1131P, 45 more genes
    nsv5359075translocation1nstd200human GRCh38 chr18: 47,131,723-47,131,723 , GRCh38 chr18: 47,131,672-47,131,672 , GRCh37.p13 chr18: 44,658,043-44,658,043 , GRCh37.p13 chr18: 44,658,094-44,658,094 HDHD2
    nsv5156357mobile element insertion1nstd203human GRCh38 chr18: 47,115,505-47,115,523 , GRCh37.p13 chr18: 44,641,876-44,641,894 HDHD2
    nsv5147648mobile element insertion1nstd203human GRCh38 chr18: 47,115,512-47,115,523 , GRCh37.p13 chr18: 44,641,883-44,641,894 HDHD2
    nsv4757418insertion1nstd199human GRCh37 chr18: 44,641,877-44,641,877 , GRCh38.p12 chr18: 47,115,506-47,115,506 HDHD2
    nsv4725856insertion1nstd186human GRCh37 chr18: 44,641,876-44,641,876 , GRCh38.p12 chr18: 47,115,505-47,115,505 HDHD2
    nsv4690737mobile element insertion1nstd186human GRCh37 chr18: 44,641,894-44,641,894 , GRCh38.p12 chr18: 47,115,523-47,115,523 HDHD2
    nsv4676219copy number variation1nstd102humanPathogenic GRCh37 chr18: 41,630,585-45,107,905 , GRCh38.p12 chr18: 44,050,620-47,581,534 HAUS1, KATNAL2, 48 more genes
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
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