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Items: 1 to 20 of 322

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123710insertion1nstd186human GRCh37 chr4: 99,818,441-99,818,477 , GRCh38.p12 chr4: 98,897,290-98,897,326 EIF4E
    nsv5955044insertion1nstd209human GRCh38 chr4: 98,896,224-98,896,224 , GRCh37.p13 chr4: 99,817,375-99,817,375 EIF4E
    nsv5906671copy number variation1nstd209human GRCh38 chr4: 98,892,636-98,895,947 , GRCh37.p13 chr4: 99,813,787-99,817,098 EIF4E
    nsv5840235copy number variation1nstd209human GRCh38 chr4: 98,892,649-98,896,091 , GRCh37.p13 chr4: 99,813,800-99,817,242 EIF4E
    nsv5624383insertion1nstd207human GRCh38 chr4: 98,893,148-98,893,148 , GRCh37.p13 chr4: 99,814,299-99,814,299 EIF4E
    nsv5612004insertion1nstd207human GRCh38 chr4: 98,896,224-98,896,224 , GRCh37.p13 chr4: 99,817,375-99,817,375 EIF4E
    nsv5607156insertion1nstd207human GRCh38 chr4: 98,895,092-98,895,092 , GRCh37.p13 chr4: 99,816,243-99,816,243 EIF4E
    nsv5606439insertion1nstd207human GRCh38 chr4: 98,897,275-98,897,275 , GRCh37.p13 chr4: 99,818,426-99,818,426 EIF4E
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5536836insertion1nstd206human GRCh38 chr4: 98,897,290-98,897,326 , GRCh37.p13 chr4: 99,818,441-99,818,477 EIF4E
    nsv5467864copy number variation1nstd206human GRCh38 chr4: 98,876,850-98,879,546 , GRCh37.p13 chr4: 99,798,001-99,800,697 EIF4E
    nsv5454496copy number variation1nstd206human GRCh38 chr4: 98,892,636-98,895,949 , GRCh37.p13 chr4: 99,813,787-99,817,100 EIF4E
    nsv5386681copy number variation2nstd186human GRCh37 chr4: 99,813,787-99,817,100 , GRCh38.p12 chr4: 98,892,636-98,895,949 EIF4E
    nsv5346903translocation1nstd200human GRCh38 chr4: 98,881,232-98,881,232 , GRCh38 chr4: 98,881,736-98,881,736 , GRCh37.p13 chr4: 99,802,383-99,802,383 , GRCh37.p13 chr4: 99,802,887-99,802,887 EIF4E
    nsv5317699copy number variation1nstd204human GRCh38.p13 chr4: 98,918,188-98,922,399 , GRCh37.p13 chr4: 99,839,339-99,843,550 EIF4E
    nsv5315839copy number variation1nstd204human GRCh38.p13 chr4: 98,892,636-98,895,949 , GRCh37.p13 chr4: 99,813,787-99,817,100 EIF4E
    nsv5311203copy number variation1nstd204human GRCh38.p13 chr4: 98,465,397-99,287,870 , GRCh37.p13 chr4: 99,386,548-100,209,027 TBCAP3, ADH5, 19 more genes
    nsv5239886copy number variation1nstd204human GRCh38.p13 chr4: 98,506,801-99,288,000 , GRCh37.p13 chr4: 99,427,952-100,209,157 TSPAN5, PCNAP1, 19 more genes
    nsv5238250copy number variation1nstd204human GRCh38.p13 chr4: 98,892,601-98,896,800 , GRCh37.p13 chr4: 99,813,752-99,817,951 EIF4E
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