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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7046833inversion1nstd229human GRCh37.p13 chr1|NW_003871055.3: 6,618,859-6,664,070 , GRCh38 chr1: 149,803,446-149,848,657 , GRCh37.p13 chr1: 149,775,002-149,820,224 H2BC19P, H3C13, 5 more genes
    nsv6333655copy number variation1nstd223human GRCh38 chr1: 149,791,101-149,793,900 , GRCh37.p13 chr1: 149,762,657-149,765,456 , GRCh37.p13 chr1|NW_003871055.3: 6,606,514-6,609,313 FCGR1A, H2BC18
    nsv6296875copy number variation1nstd186human GRCh37 chr1: 149,783,555-149,792,142 , GRCh38.p12 chr1: 149,812,000-149,820,587 H3C13, H2BC18
    nsv6133732copy number variation1nstd213human GRCh37 chr1: 149,750,000-153,310,001 , GRCh38.p12 chr1: 149,778,444-153,337,525 , CTSK, 183 more genes
    nsv5867973copy number variation1nstd209human GRCh38 chr1: 149,793,568-149,796,164 , GRCh37.p13 chr1|NW_003871055.3: 6,608,981-6,611,577 , GRCh37.p13 chr1: 149,765,124-149,767,720 H2BC18
    nsv5828343copy number variation1nstd209human GRCh37.p13 chr1|NW_003871055.3: 6,595,690-6,631,896 , GRCh38 chr1: 149,780,277-149,816,483 , GRCh37.p13 chr1: 149,751,833-149,788,037 FCGR1A, H2BC18, 1 more genes
    nsv5828226copy number variation1nstd209human GRCh38 chr1: 149,786,287-149,789,021 , GRCh37.p13 chr1: 149,757,843-149,760,577 , GRCh37.p13 chr1|NW_003871055.3: 6,601,700-6,604,434 FCGR1A, H2BC18
    nsv5622478insertion1nstd207human GRCh38 chr1: 149,810,921-149,810,921 , GRCh37.p13 chr1: 149,782,476-149,782,476 , GRCh37.p13 chr1|NW_003871055.3: 6,626,334-6,626,334 H2BC18
    nsv5576553copy number variation1nstd207human GRCh38 chr1: 149,801,061-149,801,146 , GRCh37.p13 chr1: 149,772,617-149,772,702 , GRCh37.p13 chr1|NW_003871055.3: 6,616,474-6,616,559 H2BC18
    nsv5431757copy number variation1nstd206human GRCh38 chr1: 149,784,587-149,802,587 , GRCh37.p13 chr1|NW_003871055.3: 6,600,000-6,618,000 , GRCh37.p13 chr1: 149,756,143-149,774,143 FCGR1A, H2BC18
    nsv5426258copy number variation1nstd206human GRCh38 chr1: 149,812,000-149,820,587 , GRCh37.p13 chr1|NW_003871055.3: 6,627,413-6,636,000 , GRCh37.p13 chr1: 149,783,555-149,792,142 H2BC18, H3C13
    nsv5424510copy number variation1nstd206human GRCh38 chr1: 149,793,548-149,796,182 , GRCh37.p13 chr1: 149,765,104-149,767,738 , GRCh37.p13 chr1|NW_003871055.3: 6,608,961-6,611,595 H2BC18
    nsv5421829copy number variation1nstd206human GRCh38 chr1: 149,801,800-149,822,587 , GRCh37.p13 chr1|NW_003871055.3: 6,617,213-6,638,000 , GRCh37.p13 chr1: 149,773,356-149,794,142 H2BC18, H3C13
    nsv5421806copy number variation1nstd206human GRCh38 chr1: 149,782,587-149,789,000 , GRCh37.p13 chr1|NW_003871055.3: 6,598,000-6,604,413 , GRCh37.p13 chr1: 149,754,143-149,760,556 H2BC18, FCGR1A
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5216716copy number variation1nstd204human GRCh38.p13 chr1: 149,809,601-149,810,100 , GRCh37.p13 chr1: 149,781,156-149,781,655 , GRCh37.p13 chr1|NW_003871055.3: 6,625,014-6,625,513 H2BC18
    nsv5207690copy number variation1nstd204human GRCh38.p13 chr1: 149,810,379-149,813,294 , GRCh37.p13 chr1|NW_003871055.3: 6,625,792-6,628,707 , GRCh37.p13 chr1: 149,781,934-149,784,849 H3C13, H2BC18
    nsv4773942copy number variation1nstd200human GRCh37 chr1: 149,764,901-149,767,721 , GRCh38.p12 chr1: 149,793,345-149,796,165 H2BC18
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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