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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
    nsv7077542inversion1nstd229human GRCh38 chr12: 7,565,102-9,354,075 , GRCh37.p13 chr12: 7,717,698-9,506,671 ALG1L10P, RPL15P17, 69 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
    nsv7074407inversion1nstd229human GRCh38 chr12: 7,895,385-8,483,851 , GRCh37.p13 chr12: 8,047,981-8,636,447 SNRPCP7, NANOGP1, 29 more genes
    nsv7072396inversion1nstd229human GRCh38 chr12: 8,023,307-8,392,436 , GRCh37.p13 chr12: 8,175,903-8,545,032 FAM90A1, POU5F1P3, 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
    nsv7068010inversion1nstd229human GRCh38 chr12: 7,025,778-10,225,656 , GRCh37.p13 chr12: 7,178,850-10,378,255 GOT2P3, CLEC2B, 123 more genes
    nsv7064008inversion1nstd229human GRCh38 chr12: 6,716,253-10,225,825 , GRCh37.p13 chr12: 6,825,419-10,378,424 PTMAP4, COPS7A, 153 more genes
    nsv6931418copy number variation1nstd229human GRCh38 chr12: 8,208,854-8,238,302 , GRCh37.p13 chr12: 8,361,450-8,390,898 FAM90A1, LINC02449, 3 more genes
    nsv6927052copy number variation1nstd229human GRCh38 chr12: 8,217,656-8,229,186 , GRCh37.p13 chr12: 8,370,252-8,381,782 FAM90A1, DEFB109F, 2 more genes
    nsv6924164copy number variation1nstd229human GRCh38 chr12: 8,126,744-8,525,670 , GRCh37.p13 chr12: 8,279,340-8,678,266 POU5F1P3, LINC02449, 23 more genes
    nsv6923100copy number variation1nstd229human GRCh38 chr12: 8,236,549-8,236,683 , GRCh37.p13 chr12: 8,389,145-8,389,279 LINC02449, FAM86FP
    nsv6621755copy number variation1nstd224human GRCh37 chr12: 8,376,070-8,509,576 , GRCh38.p12 chr12: 8,223,474-8,356,980 FAM90A1, LINC00937, 7 more genes
    nsv6621754copy number variation1nstd224human GRCh37 chr12: 8,374,746-8,509,669 , GRCh38.p12 chr12: 8,222,150-8,357,073 FAM86FP, SNRPCP7, 9 more genes
    nsv6621753copy number variation2nstd224human GRCh37 chr12: 8,374,746-8,394,377 , GRCh38.p12 chr12: 8,222,150-8,241,781 FAM86FP, LINC02449, 2 more genes
    nsv6473973copy number variation1nstd223human GRCh38 chr12: 8,208,701-8,245,000 , GRCh37.p13 chr12: 8,361,297-8,397,596 LINC02449, FAM90A1, 4 more genes
    nsv6472933copy number variation1nstd223human GRCh38 chr12: 8,208,801-8,230,400 , GRCh37.p13 chr12: 8,361,397-8,382,996 ALG1L10P, FAM90A1, 2 more genes
    nsv6466746copy number variation1nstd223human GRCh38 chr12: 8,227,001-8,238,300 , GRCh37.p13 chr12: 8,379,597-8,390,896 FAM86FP, LINC02449, 2 more genes
    nsv6466713copy number variation1nstd223human GRCh38 chr12: 8,225,901-8,238,400 , GRCh37.p13 chr12: 8,378,497-8,390,996 FAM86FP, LINC02449, 2 more genes
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