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Items: 1 to 20 of 524

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 more genes
    nsv7059324inversion1nstd229human GRCh38 chr13: 28,207,371-28,214,380 , GRCh37.p13 chr13: 28,781,508-28,788,517 EEF1A1P3, PAN3
    nsv6936638copy number variation1nstd229human GRCh38 chr13: 28,147,150-28,147,765 , GRCh37.p13 chr13: 28,721,287-28,721,902 PAN3
    nsv6934639copy number variation1nstd229human GRCh38 chr13: 28,184,833-28,289,437 , GRCh37.p13 chr13: 28,758,970-28,863,574 EEF1A1P3, RNU6-82P, 1 more genes
    nsv6933390copy number variation1nstd229human GRCh38 chr13: 28,155,501-28,159,800 , GRCh37.p13 chr13: 28,729,638-28,733,937 PAN3
    nsv6932123copy number variation1nstd229human GRCh38 chr13: 28,158,361-28,159,290 , GRCh37.p13 chr13: 28,732,498-28,733,427 PAN3
    nsv6932013copy number variation1nstd229human GRCh38 chr13: 27,894,801-28,169,500 , GRCh37.p13 chr13: 28,468,938-28,743,637 URAD, CDX2, 12 more genes
    nsv6930889copy number variation1nstd229human GRCh38 chr13: 28,210,323-28,212,738 , GRCh37.p13 chr13: 28,784,460-28,786,875 EEF1A1P3, PAN3
    nsv6930670copy number variation1nstd229human GRCh38 chr13: 28,188,601-28,206,300 , GRCh37.p13 chr13: 28,762,738-28,780,437 PAN3
    nsv6925127copy number variation1nstd229human GRCh38 chr13: 28,171,901-28,174,100 , GRCh37.p13 chr13: 28,746,038-28,748,237 PAN3
    nsv6924945copy number variation1nstd229human GRCh38 chr13: 28,200,068-28,200,236 , GRCh37.p13 chr13: 28,774,205-28,774,373 PAN3
    nsv6923663copy number variation1nstd229human GRCh38 chr13: 28,289,605-28,290,482 , GRCh37.p13 chr13: 28,863,742-28,864,619 PAN3
    nsv6922692copy number variation1nstd229human GRCh38 chr13: 28,119,609-28,133,363 , GRCh37.p13 chr13: 28,693,746-28,707,500 PAN3
    nsv6922545copy number variation1nstd229human GRCh38 chr13: 28,243,256-28,251,789 , GRCh37.p13 chr13: 28,817,393-28,825,926 PAN3
    nsv6921151copy number variation1nstd229human GRCh38 chr13: 28,143,288-28,150,875 , GRCh37.p13 chr13: 28,717,425-28,725,012 PAN3
    nsv6920228copy number variation1nstd229human GRCh38 chr13: 28,256,901-28,266,100 , GRCh37.p13 chr13: 28,831,038-28,840,237 PAN3
    nsv6919531copy number variation1nstd229human GRCh38 chr13: 28,265,729-28,266,044 , GRCh37.p13 chr13: 28,839,866-28,840,181 PAN3
    nsv6918144copy number variation1nstd229human GRCh38 chr13: 28,132,663-28,276,868 , GRCh37.p13 chr13: 28,706,800-28,851,005 EEF1A1P3, PAN3, 2 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6590576inversion1nstd223human GRCh38 chr13: 28,197,762-28,198,295 , GRCh37.p13 chr13: 28,771,899-28,772,432 PAN3
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