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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7094735copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,465,346-80,465,496 , GRCh38.p12 chr15: 80,173,004-80,173,154 FAH
    nsv7094636copy number variation1nstd102humanUncertain significance GRCh37 chr15: 78,857,986-81,282,132 , GRCh38.p12 chr15: 78,565,644-80,989,791 LOC646934, RNU6-415P, 51 more genes
    nsv7076478inversion1nstd229human GRCh38 chr15: 79,261,836-81,280,491 , GRCh37.p13 chr15: 79,554,178-81,572,832 CFAP161, TMED3, 34 more genes
    nsv7063463inversion1nstd229human GRCh38 chr15: 75,234,241-81,337,543 , GRCh37.p13 chr15: 75,526,582-81,629,884 RN7SL327P, LOC105370910, 138 more genes
    nsv7062055inversion1nstd229human GRCh38 chr15: 72,671,162-80,404,440 , GRCh37.p13 chr15: 72,963,503-80,696,782 MIR184, TRK-CTT16-1, 194 more genes
    nsv6977661copy number variation1nstd229human GRCh38 chr15: 80,161,797-80,174,871 , GRCh37.p13 chr15: 80,454,139-80,467,213 FAH
    nsv6971439copy number variation1nstd229human GRCh38 chr15: 80,178,172-80,181,249 , GRCh37.p13 chr15: 80,470,514-80,473,591 FAH
    nsv6969044copy number variation1nstd229human GRCh38 chr15: 77,623,918-81,694,021 , GRCh37.p13 chr15: 77,916,260-81,986,362 ST20-MTHFS, CSPG4P13, 87 more genes
    nsv6961188copy number variation1nstd229human GRCh38 chr15: 80,165,858-80,170,581 , GRCh37.p13 chr15: 80,458,200-80,462,923 FAH
    nsv6960220copy number variation1nstd229human GRCh38 chr15: 80,180,588-80,189,520 , GRCh37.p13 chr15: 80,472,930-80,481,862 FAH
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6637608copy number variation1nstd102humanUncertain significance GRCh37 chr15: 79,996,626-82,097,796 , GRCh38.p12 chr15: 79,704,284-81,805,455 ARNT2, LOC105370921, 31 more genes
    nsv6579530inversion1nstd223human GRCh38 chr15: 77,618,605-83,035,894 , GRCh37.p13 chr15: 77,910,947-83,704,646 CIB2, TFDP1P3, 127 more genes
    nsv6579525inversion1nstd223human GRCh38 chr15: 77,618,608-83,164,280 , GRCh37.p13 chr15: 77,910,950-83,833,032 STARD5, RPL9P8, 131 more genes
    nsv6578911inversion1nstd223human GRCh38 chr15: 77,618,608-84,708,062 , GRCh37.p13 chr15: 77,910,950-85,251,293 TMC3-AS1, LOC642677, 177 more genes
    nsv6497689copy number variation1nstd223human GRCh38 chr15: 80,166,241-80,167,362 , GRCh37.p13 chr15: 80,458,583-80,459,704 FAH
    nsv6315271copy number variation1nstd102humanLikely benign GRCh38 chr15: 80,152,696-80,152,761 , GRCh37 chr15: 80,445,038-80,445,103 FAH
    nsv6309827copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,450,392-80,454,688 , GRCh38.p12 chr15: 80,158,050-80,162,346 FAH
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