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Items: 1 to 20 of 164

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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
    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
    nsv7074628inversion1nstd229human GRCh38 chr12: 5,173,229-8,663,348 , GRCh37.p13 chr12: 5,282,395-8,815,944 P3H3, LOC105369621, 141 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
    nsv6933605copy number variation1nstd229human GRCh38 chr12: 5,238,980-5,244,329 , GRCh37.p13 chr12: 5,348,146-5,353,495 LINC02443, LOC105369617
    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
    nsv6924501copy number variation1nstd229human GRCh38 chr12: 5,222,722-5,947,811 , GRCh37.p13 chr12: 5,331,888-6,056,977 VWF, LOC101901829, 6 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
    nsv6621809copy number variation1nstd224human GRCh37 chr12: 5,241,721-5,392,819 , GRCh38.p12 chr12: 5,132,555-5,283,653 LINC02443, LOC105369617, 1 more genes
    nsv6590771inversion1nstd223human GRCh38 chr12: 4,721,937-5,537,202 , GRCh37.p13 chr12: 4,831,103-5,646,368 KCNA1, KCNA6, 9 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
    nsv6465944copy number variation1nstd223human GRCh38 chr12: 5,241,530-5,242,014 , GRCh37.p13 chr12: 5,350,696-5,351,180 LINC02443, LOC105369617
    nsv6290254copy number variation1nstd102humanPathogenic GRCh37 chr12: 146,240-8,330,229 , GRCh38.p12 chr12: 45,740-8,177,633 CLEC4A, FBXL14, 220 more genes
    nsv6132693copy number variation1nstd213human GRCh37 chr12: 3,310,000-5,630,001 , GRCh38.p12 chr12: 3,200,834-5,520,835 CCND2, FGF6, 44 more genes
    nsv6132596copy number variation1nstd213human GRCh37 chr12: 5,190,000-5,830,001 , GRCh38.p12 chr12: 5,080,834-5,720,835 NTF3, ANO2, 5 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132253copy number variation1nstd213human GRCh37 chr12: 5,310,000-5,670,001 , GRCh38.p12 chr12: 5,200,834-5,560,835 NTF3, ANO2, 4 more genes
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
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