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Items: 1 to 20 of 306

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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
    nsv6937899copy number variation1nstd229human GRCh38 chr12: 4,658,781-4,746,281 , GRCh37.p13 chr12: 4,767,947-4,855,447 GALNT8, NDUFA9, 1 more genes
    nsv6935956copy number variation1nstd229human GRCh38 chr12: 4,618,910-4,651,921 , GRCh37.p13 chr12: 4,728,076-4,761,087 NDUFA9, AKAP3, 1 more genes
    nsv6932905copy number variation1nstd229human GRCh38 chr12: 4,651,753-4,656,836 , GRCh37.p13 chr12: 4,760,919-4,766,002 NDUFA9
    nsv6931417copy number variation1nstd229human GRCh38 chr12: 4,658,665-4,658,853 , GRCh37.p13 chr12: 4,767,831-4,768,019 NDUFA9
    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
    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
    nsv6922974copy number variation1nstd229human GRCh38 chr12: 4,658,601-4,678,400 , GRCh37.p13 chr12: 4,767,767-4,787,566 NDUFA9
    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
    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
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6621702copy number variation1nstd224human GRCh37 chr12: 4,768,306-4,855,393 , GRCh38.p12 chr12: 4,659,140-4,746,227 NDUFA9, GALNT8, 1 more genes
    nsv6473617copy number variation1nstd223human GRCh38 chr12: 3,972,756-5,647,610 , GRCh37.p13 chr12: 4,081,922-5,756,776 KCNA5, LINC02443, 29 more genes
    nsv6463108copy number variation1nstd223human GRCh38 chr12: 4,667,008-4,667,714 , GRCh37.p13 chr12: 4,776,174-4,776,880 NDUFA9
    nsv6313933copy number variation1nstd102humanPathogenic GRCh37 chr12: 2,790,077-5,325,700 , GRCh38.p12 chr12: 2,680,911-5,216,534 OTUD4P1, DYRK4, 59 more genes
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