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Items: 1 to 20 of 215

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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
    nsv7094156copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,211,333-8,248,686 , GRCh38.p12 chr12: 8,058,737-8,096,090 NECAP1, C3AR1
    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
    nsv6937134copy number variation1nstd229human GRCh38 chr12: 8,090,019-8,095,000 , GRCh37.p13 chr12: 8,242,615-8,247,596 NECAP1
    nsv6919847copy number variation1nstd229human GRCh38 chr12: 7,812,181-8,115,584 , GRCh37.p13 chr12: 7,964,777-8,268,180 LOC100462988, CLEC4A, 10 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
    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
    nsv6587830inversion1nstd223human GRCh38 chr12: 8,085,959-8,086,489 , GRCh37.p13 chr12: 8,238,555-8,239,085 NECAP1
    nsv6577830inversion1nstd223human GRCh38 chr12: 8,085,933-8,086,481 , GRCh37.p13 chr12: 8,238,529-8,239,077 NECAP1
    nsv6457638copy number variation1nstd223human GRCh38 chr12: 8,090,019-8,094,997 , GRCh37.p13 chr12: 8,242,615-8,247,593 NECAP1
    nsv6309517copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,248,177-8,248,319 , GRCh38.p12 chr12: 8,095,581-8,095,723 NECAP1
    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
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