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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902745copy number variation1nstd209human GRCh38 chr6: 57,023,652-57,023,804 , GRCh37.p13 chr6: 56,888,450-56,888,602 BEND6
    nsv5679362mobile element insertion2nstd211human GRCh38 chr6: 57,016,732-57,016,732 , GRCh37.p13 chr6: 56,881,530-56,881,530 BEND6
    nsv5674593mobile element insertion1nstd211human GRCh38 chr6: 57,020,854-57,020,854 , GRCh37.p13 chr6: 56,885,652-56,885,652 BEND6
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5462293copy number variation1nstd206human GRCh38 chr6: 57,018,830-57,018,939 , GRCh37.p13 chr6: 56,883,628-56,883,737 BEND6
    nsv5395170mobile element insertion1nstd206human GRCh38 chr6: 57,016,732-57,016,783 , GRCh37.p13 chr6: 56,881,530-56,881,581 BEND6
    nsv5184499mobile element insertion1nstd203human GRCh38 chr6: 57,009,992-57,010,005 , GRCh37.p13 chr6: 56,874,790-56,874,803 BEND6
    nsv5116579mobile element insertion1nstd203human GRCh38 chr6: 56,984,584-56,984,597 , GRCh37.p13 chr6: 56,849,382-56,849,395 BEND6
    nsv4947788copy number variation1nstd200human GRCh38 chr6: 57,013,191-57,061,645 , GRCh37.p13 chr6: 56,877,989-56,926,443 MRPL30P1, KIAA1586, 1 more genes
    nsv4947787copy number variation1nstd200human GRCh38 chr6: 57,003,944-57,008,756 , GRCh37.p13 chr6: 56,868,742-56,873,554 FTH1P15, BEND6
    nsv4947786copy number variation1nstd200human GRCh38 chr6: 56,998,282-56,998,571 , GRCh37.p13 chr6: 56,863,080-56,863,369 BEND6
    nsv4947785copy number variation1nstd200human GRCh38 chr6: 56,979,608-57,010,340 , GRCh37.p13 chr6: 56,844,406-56,875,138 FTH1P15, BEND6
    nsv4934764copy number variation1nstd200human GRCh38 chr6: 57,005,538-57,030,390 , GRCh37.p13 chr6: 56,870,336-56,895,188 BEND6, MRPL30P1
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4592867copy number variation1nstd183human GRCh37 chr6: 56,878,153-56,905,274 , GRCh38.p12 chr6: 57,013,355-57,040,476 MRPL30P1, BEND6
    nsv4481092mobile element insertion1nstd166human GRCh37.p13 chr6: 56,849,382-56,849,382 , GRCh38.p12 chr6: 56,984,584-56,984,584 BEND6
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4151459copy number variation1nstd166human GRCh37.p13 chr6: 56,888,452-56,888,603 , GRCh38.p12 chr6: 57,023,654-57,023,805 BEND6
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