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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044079inversion1nstd229human GRCh38 chr1: 174,711,171-179,623,233 , GRCh37.p13 chr1: 174,680,309-179,592,368 LOC100420262, RNU6-307P, 71 more genes
    nsv7039025inversion1nstd229human GRCh38 chr1: 177,358,419-177,359,249 , GRCh37.p13 chr1: 177,327,555-177,328,385 LINC01645
    nsv6645433copy number variation1nstd229human GRCh38 chr1: 177,364,103-177,380,262 , GRCh37.p13 chr1: 177,333,239-177,349,398 LINC01645
    nsv6645432copy number variation1nstd229human GRCh38 chr1: 177,359,846-177,391,567 , GRCh37.p13 chr1: 177,328,982-177,360,703 LINC01645
    nsv6645431copy number variation1nstd229human GRCh38 chr1: 177,354,164-177,354,195 , GRCh37.p13 chr1: 177,323,300-177,323,331 LINC01645
    nsv6645380copy number variation1nstd229human GRCh38 chr1: 177,343,198-177,740,948 , GRCh37.p13 chr1: 177,312,334-177,710,083 LINC01741, LINC01645
    nsv6645289copy number variation1nstd229human GRCh38 chr1: 177,345,601-177,349,800 , GRCh37.p13 chr1: 177,314,737-177,318,936 LINC01645
    nsv6331476copy number variation1nstd223human GRCh38 chr1: 177,361,501-177,363,100 , GRCh37.p13 chr1: 177,330,637-177,332,236 LINC01645
    nsv6330654copy number variation1nstd223human GRCh38 chr1: 177,364,103-177,380,255 , GRCh37.p13 chr1: 177,333,239-177,349,391 LINC01645
    nsv6292241mobile element insertion1nstd186human GRCh37 chr1: 177,323,813-177,323,864 , GRCh38.p12 chr1: 177,354,677-177,354,728 LINC01645
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133835copy number variation1nstd213human GRCh37 chr1: 177,040,000-182,410,001 , GRCh38.p12 chr1: 177,070,864-182,440,866 VDAC1P4, RASAL2, 92 more genes
    nsv6133834copy number variation1nstd213human GRCh37 chr1: 176,040,000-177,510,001 , GRCh38.p12 chr1: 176,070,864-177,540,866 PAPPA2, COP1, 10 more genes
    nsv6133601copy number variation1nstd213human GRCh37 chr1: 177,240,000-177,430,001 , GRCh38.p12 chr1: 177,270,864-177,460,865 BRINP2, LINC01645
    nsv6133573copy number variation1nstd213human GRCh37 chr1: 173,820,000-189,960,001 , GRCh38.p12 chr1: 173,850,862-189,990,871 ABL2, ASTN1, 235 more genes
    nsv5689977mobile element insertion1nstd211human GRCh38 chr1: 177,364,906-177,364,906 , GRCh37.p13 chr1: 177,334,042-177,334,042 LINC01645
    nsv5685074mobile element insertion1nstd211human GRCh38 chr1: 177,354,677-177,354,677 , GRCh37.p13 chr1: 177,323,813-177,323,813 LINC01645
    nsv5411612mobile element insertion1nstd206human GRCh38 chr1: 177,354,677-177,354,728 , GRCh37.p13 chr1: 177,323,813-177,323,864 LINC01645
    nsv5397484mobile element insertion1nstd206human GRCh38 chr1: 177,364,906-177,364,957 , GRCh37.p13 chr1: 177,334,042-177,334,093 LINC01645
    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
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