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Items: 1 to 20 of 249

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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
    nsv6931000copy number variation1nstd229human GRCh38 chr12: 8,195,443-8,197,599 , GRCh37.p13 chr12: 8,348,039-8,350,195 FAM66C, DEFB109F
    nsv6927515copy number variation1nstd229human GRCh38 chr12: 8,183,394-8,183,436 , GRCh37.p13 chr12: 8,335,990-8,336,032 FAM66C
    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
    nsv6918242copy number variation1nstd229human GRCh38 chr12: 8,142,764-8,195,071 , GRCh37.p13 chr12: 8,295,360-8,347,667 ZNF705A, FAM66C, 1 more genes
    nsv6621877copy number variation1nstd224human GRCh37 chr12: 7,832,447-8,374,746 , GRCh38.p12 chr12: 7,679,851-8,222,150 GDF3, NECAP1, 21 more genes
    nsv6471383copy number variation1nstd223human GRCh38 chr12: 8,200,701-8,202,600 , GRCh37.p13 chr12: 8,353,297-8,355,196 DEFB109F, FAM66C
    nsv6309483copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-8,756,953 , GRCh38.p12 chr12: 6,329,312-8,604,357 ENPP7P5, GPR162, 122 more genes
    nsv6309328copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,978,008-9,010,204 , GRCh38.p12 chr12: 6,868,844-8,857,608 LOC101927966, SNRPCP7, 87 more genes
    nsv6195970copy number variation1nstd214human GRCh38 chr12: 8,183,812-8,183,887 , GRCh37.p13 chr12: 8,336,408-8,336,483 FAM66C
    nsv6132616copy number variation1nstd213human GRCh37 chr12: 8,100,000-12,900,001 , GRCh38.p12 chr12: 7,947,404-12,747,067 A2M, A2MP1, 178 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
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