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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7073282inversion1nstd229human GRCh38 chr10: 12,099,288-14,830,781 , GRCh37.p13 chr10: 12,141,287-14,872,780 MIR1265, RNA5SP301, 45 more genes
    nsv7072913inversion1nstd229human GRCh38 chr10: 13,339,827-13,340,006 , GRCh37.p13 chr10: 13,381,827-13,382,006 SEPHS1
    nsv7061969inversion1nstd229human GRCh38 chr10: 11,128,019-14,526,691 , GRCh37.p13 chr10: 11,169,982-14,568,690 RPL5P25, LOC105376425, 58 more genes
    nsv7060184inversion1nstd229human GRCh38 chr10: 13,148,010-16,128,795 , GRCh37.p13 chr10: 13,190,010-16,170,794 LOC101928453, MCM10, 52 more genes
    nsv6884753copy number variation1nstd229human GRCh38 chr10: 13,325,912-13,325,962 , GRCh37.p13 chr10: 13,367,912-13,367,962 SEPHS1
    nsv6620178copy number variation1nstd224human GRCh37 chr10: 13,387,295-13,534,851 , GRCh38.p12 chr10: 13,345,295-13,492,851 BEND7, SEPHS1, 2 more genes
    nsv6592458inversion1nstd223human GRCh38 chr10: 11,934,638-13,951,892 , GRCh37.p13 chr10: 11,976,637-13,993,892 RNU6-6P, MIR548Q, 38 more genes
    nsv6587557inversion1nstd223human GRCh38 chr10: 13,342,384-13,342,989 , GRCh37.p13 chr10: 13,384,384-13,384,989 SEPHS1
    nsv6576689inversion1nstd223human GRCh38 chr10: 13,342,238-13,342,795 , GRCh37.p13 chr10: 13,384,238-13,384,795 SEPHS1
    nsv6445663copy number variation1nstd223human GRCh38 chr10: 13,323,456-13,324,695 , GRCh37.p13 chr10: 13,365,456-13,366,695 SEPHS1
    nsv6435833copy number variation1nstd223human GRCh38 chr10: 13,346,501-13,348,500 , GRCh37.p13 chr10: 13,388,501-13,390,500 SEPHS1
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6131971copy number variation1nstd213human GRCh37 chr10: 7,450,000-17,830,001 , GRCh38.p12 chr10: 7,408,038-17,788,002 ATP5F1C, TRDMT1, 150 more genes
    nsv5911740copy number variation1nstd209human GRCh38 chr10: 13,345,026-13,347,996 , GRCh37.p13 chr10: 13,387,026-13,389,996 SEPHS1
    nsv5701375mobile element insertion1nstd211human GRCh38 chr10: 13,316,701-13,316,701 , GRCh37.p13 chr10: 13,358,701-13,358,701 SEPHS1
    nsv5700155mobile element insertion1nstd211human GRCh38 chr10: 13,326,961-13,326,961 , GRCh37.p13 chr10: 13,368,961-13,368,961 SEPHS1
    nsv5553139insertion1nstd206human GRCh38 chr10: 13,326,961-13,327,001 , GRCh37.p13 chr10: 13,368,961-13,369,001 SEPHS1
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