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Items: 1 to 20 of 202

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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
    nsv7073282inversion1nstd229human GRCh38 chr10: 12,099,288-14,830,781 , GRCh37.p13 chr10: 12,141,287-14,872,780 MIR1265, RNA5SP301, 45 more genes
    nsv7069439inversion1nstd229human GRCh38 chr10: 10,500,497-12,439,947 , GRCh37.p13 chr10: 10,542,460-12,481,946 LOC105376409, SFTA1P, 26 more genes
    nsv7061969inversion1nstd229human GRCh38 chr10: 11,128,019-14,526,691 , GRCh37.p13 chr10: 11,169,982-14,568,690 RPL5P25, LOC105376425, 58 more genes
    nsv7058695inversion1nstd229human GRCh38 chr10: 11,787,108-13,297,144 , GRCh37.p13 chr10: 11,829,107-13,339,144 RNU6-6P, SEC61A2, 28 more genes
    nsv6894218copy number variation1nstd229human GRCh38 chr10: 12,171,795-12,174,956 , GRCh37.p13 chr10: 12,213,794-12,216,955 NUDT5
    nsv6892932copy number variation1nstd229human GRCh38 chr10: 12,120,615-12,475,512 , GRCh37.p13 chr10: 12,162,614-12,517,511 CAMK1D, CDC123, 7 more genes
    nsv6891220copy number variation1nstd229human GRCh38 chr10: 12,182,110-12,188,268 , GRCh37.p13 chr10: 12,224,109-12,230,267 NUDT5
    nsv6887574copy number variation1nstd229human GRCh38 chr10: 12,157,973-12,742,581 , GRCh37.p13 chr10: 12,199,972-12,784,580 RN7SL198P, SEC61A2, 8 more genes
    nsv6882948copy number variation1nstd229human GRCh38 chr10: 12,194,376-12,198,186 , GRCh37.p13 chr10: 12,236,375-12,240,185 CDC123, NUDT5
    nsv6637939copy number variation1nstd102humanUncertain significance GRCh37 chr10: 100,027-12,648,149 , GRCh38.p12 chr10: 54,087-12,606,150 LARP4B-DT, CALML5, 206 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
    nsv6591083inversion1nstd223human GRCh38 chr10: 12,181,807-12,182,775 , GRCh37.p13 chr10: 12,223,806-12,224,774 NUDT5
    nsv6580803inversion1nstd223human GRCh38 chr10: 12,119,024-12,302,659 , GRCh37.p13 chr10: 12,161,023-12,344,658 CDC123, NUDT5, 3 more genes
    nsv6578932inversion1nstd223human GRCh38 chr10: 12,187,482-12,187,631 , GRCh37.p13 chr10: 12,229,481-12,229,630 NUDT5
    nsv6576329inversion1nstd223human GRCh38 chr10: 12,181,936-12,183,013 , GRCh37.p13 chr10: 12,223,935-12,225,012 NUDT5
    nsv6449592copy number variation1nstd223human GRCh38 chr10: 12,182,885-12,184,138 , GRCh37.p13 chr10: 12,224,884-12,226,137 NUDT5
    nsv6437606copy number variation1nstd223human GRCh38 chr10: 12,176,101-12,177,500 , GRCh37.p13 chr10: 12,218,100-12,219,499 NUDT5
    nsv6435971copy number variation1nstd223human GRCh38 chr10: 12,176,955-12,177,530 , GRCh37.p13 chr10: 12,218,954-12,219,529 NUDT5
    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
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