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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901102copy number variation1nstd209human GRCh38 chr2: 170,828,020-170,828,081 , GRCh37.p13 chr2: 171,684,530-171,684,591 GAD1
    nsv5892227copy number variation1nstd209human GRCh38 chr2: 170,828,975-170,829,024 , GRCh37.p13 chr2: 171,685,485-171,685,534 GAD1
    nsv5692188mobile element insertion1nstd211human GRCh38 chr2: 170,847,417-170,847,417 , GRCh37.p13 chr2: 171,703,927-171,703,927 GAD1
    nsv5684995mobile element insertion1nstd211human GRCh38 chr2: 170,844,985-170,844,985 , GRCh37.p13 chr2: 171,701,495-171,701,495 GAD1
    nsv5621592insertion1nstd207human GRCh38 chr2: 170,828,108-170,828,108 , GRCh37.p13 chr2: 171,684,618-171,684,618 GAD1
    nsv5612102insertion1nstd207human GRCh38 chr2: 170,828,296-170,828,296 , GRCh37.p13 chr2: 171,684,806-171,684,806 GAD1
    nsv5608187insertion1nstd207human GRCh38 chr2: 170,828,481-170,828,481 , GRCh37.p13 chr2: 171,684,991-171,684,991 GAD1
    nsv5571663copy number variation1nstd207human GRCh38 chr2: 170,828,555-170,828,649 , GRCh37.p13 chr2: 171,685,065-171,685,159 GAD1
    nsv5566440copy number variation1nstd207human GRCh38 chr2: 170,828,067-170,828,127 , GRCh37.p13 chr2: 171,684,577-171,684,637 GAD1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5451053copy number variation1nstd206human GRCh38 chr2: 170,801,478-170,811,857 , GRCh37.p13 chr2: 171,657,988-171,668,367 GAD1
    nsv5440607copy number variation1nstd206human GRCh38 chr2: 170,861,253-170,862,085 , GRCh37.p13 chr2: 171,717,763-171,718,595 GAD1
    nsv5411833mobile element insertion1nstd206human GRCh38 chr2: 170,844,985-170,845,036 , GRCh37.p13 chr2: 171,701,495-171,701,546 GAD1
    nsv5407347mobile element insertion1nstd206human GRCh38 chr2: 170,847,417-170,847,468 , GRCh37.p13 chr2: 171,703,927-171,703,978 GAD1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4926474copy number variation1nstd200human GRCh38 chr2: 170,861,253-170,862,085 , GRCh37.p13 chr2: 171,717,763-171,718,595 GAD1
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4789889copy number variation1nstd200human GRCh37 chr2: 171,717,763-171,718,595 , GRCh38.p12 chr2: 170,861,253-170,862,085 GAD1
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