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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056672inversion1nstd229human GRCh38 chr6: 51,226,717-52,446,371 , GRCh37.p13 chr6: 51,095,293-52,311,169 MIR206, LOC101927082, 16 more genes
    nsv6791146copy number variation1nstd229human GRCh38 chr6: 52,180,101-52,369,800 , GRCh37.p13 chr6: 52,044,899-52,234,598 MCM3, IL17A, 4 more genes
    nsv6780070copy number variation1nstd229human GRCh38 chr6: 52,186,171-52,257,901 , GRCh37.p13 chr6: 52,050,969-52,122,699 IL17F, LOC102724327, 2 more genes
    nsv6563073inversion1nstd223human GRCh38 chr6: 52,107,269-56,893,586 , GRCh37.p13 chr6: 51,972,067-56,758,384 GSTA1, LOC730101, 79 more genes
    nsv6560162inversion1nstd223human GRCh38 chr6: 52,240,266-52,241,195 , GRCh37.p13 chr6: 52,105,064-52,105,993 IL17F
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6135848copy number variation1nstd213human GRCh37 chr6: 50,080,000-52,650,001 , GRCh38.p12 chr6: 50,112,287-52,785,203 SLC25A20P1, FTH1P5, 32 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5381452copy number variation1nstd102humanUncertain significance GRCh37 chr6: 51,930,764-52,906,034 , GRCh38.p12 chr6: 52,065,966-53,041,236 GSTA4, LOC730101, 30 more genes
    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
    nsv4729270copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 48,626,041-55,575,545 , GRCh38.p12 chr6: 48,658,305-55,710,747 CRISP1, SLC25A20P1, 105 more genes
    nsv4685731copy number variation1nstd102humanPathogenic GRCh37 chr6: 51,695,623-52,371,918 , GRCh38.p12 chr6: 51,830,825-52,507,120 TRAM2, SLC25A20P1, 11 more genes
    nsv4683352copy number variation1nstd102humanUncertain significance GRCh37 chr6: 52,101,709-52,109,247 , GRCh38.p12 chr6: 52,236,911-52,244,449 SLC25A20P1, IL17F
    nsv4488039mobile element insertion1nstd166human GRCh37.p13 chr6: 52,109,087-52,109,087 , GRCh38.p12 chr6: 52,244,289-52,244,289 IL17F
    nsv4457082copy number variation1nstd102humanUncertain significance GRCh37 chr6: 51,637,152-52,303,162 , GRCh38.p12 chr6: 51,772,354-52,438,364 IL17A, PKHD1, 10 more genes
    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
    nsv4145494copy number variation1nstd166human GRCh37.p13 chr6: 52,106,858-52,108,788 , GRCh38.p12 chr6: 52,242,060-52,243,990 IL17F
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