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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7094213copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-4,796,274 , GRCh38.p12 chr12: 4,259,186-4,687,108 RPS15P7, RAD51AP1, 11 more genes
    nsv7094047copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-9,027,607 , GRCh38.p12 chr12: 4,259,186-8,875,011 ACRBP, OR7E148P, 165 more genes
    nsv7094046copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-5,155,155 , GRCh38.p12 chr12: 4,259,186-5,045,989 RPS15P7, CCND2, 18 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068624inversion1nstd229human GRCh38 chr12: 2,500,360-5,372,895 , GRCh37.p13 chr12: 2,609,526-5,482,061 LOC105369607, IQSEC3P1, 62 more genes
    nsv6937555copy number variation1nstd229human GRCh38 chr12: 4,602,533-4,602,560 , GRCh37.p13 chr12: 4,711,699-4,711,726 LOC103568124, DYRK4
    nsv6931320copy number variation1nstd229human GRCh38 chr12: 4,593,824-4,600,504 , GRCh37.p13 chr12: 4,702,990-4,709,670 LOC103568124, DYRK4
    nsv6931013copy number variation1nstd229human GRCh38 chr12: 4,335,593-4,573,659 , GRCh37.p13 chr12: 4,444,759-4,682,825 TIGAR, FGF6, 4 more genes
    nsv6930965copy number variation1nstd229human GRCh38 chr12: 4,486,494-6,353,198 , GRCh37.p13 chr12: 4,595,660-6,462,364 LOC112268088, NTF3, 34 more genes
    nsv6930188copy number variation1nstd229human GRCh38 chr12: 4,559,720-4,566,640 , GRCh37.p13 chr12: 4,668,886-4,675,806 RAD51AP1, DYRK4
    nsv6929289copy number variation1nstd229human GRCh38 chr12: 4,548,413-4,580,903 , GRCh37.p13 chr12: 4,657,579-4,690,069 RAD51AP1, DYRK4
    nsv6926233copy number variation1nstd229human GRCh38 chr12: 4,577,296-4,592,301 , GRCh37.p13 chr12: 4,686,462-4,701,467 DYRK4
    nsv6924937copy number variation1nstd229human GRCh38 chr12: 4,603,371-4,616,862 , GRCh37.p13 chr12: 4,712,537-4,726,028 AKAP3, LOC103568124, 1 more genes
    nsv6923152copy number variation1nstd229human GRCh38 chr12: 4,590,331-4,712,935 , GRCh37.p13 chr12: 4,699,497-4,822,101 AKAP3, LOC103568124, 4 more genes
    nsv6921835copy number variation1nstd229human GRCh38 chr12: 4,559,840-4,565,337 , GRCh37.p13 chr12: 4,669,006-4,674,503 DYRK4, RAD51AP1
    nsv6921708copy number variation1nstd229human GRCh38 chr12: 4,576,430-4,586,612 , GRCh37.p13 chr12: 4,685,596-4,695,778 DYRK4
    nsv6920887copy number variation1nstd229human GRCh38 chr12: 4,615,797-4,695,003 , GRCh37.p13 chr12: 4,724,963-4,804,169 DYRK4, AKAP3, 2 more genes
    nsv6920547copy number variation1nstd229human GRCh38 chr12: 4,562,579-4,562,647 , GRCh37.p13 chr12: 4,671,745-4,671,813 DYRK4
    nsv6913746copy number variation1nstd229human GRCh38 chr12: 3,972,756-5,647,610 , GRCh37.p13 chr12: 4,081,922-5,756,776 LOC101901829, LOC100420673, 29 more genes
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