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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094385copy number variation2nstd102humanPathogenic GRCh37 chr15: 50,999,997-54,025,330 , GRCh38.p12 chr15: 50,707,800-53,733,133 LOC105370826, MIR7973-2, 48 more genes
    nsv7094384copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,731,271-54,025,330 , GRCh38.p12 chr15: 50,439,074-53,733,133 LOC105370823, TMOD3, 54 more genes
    nsv7065803inversion1nstd229human GRCh38 chr15: 52,155,809-52,383,429 , GRCh37.p13 chr15: 52,448,006-52,675,626 LOC105370820, GNB5, 5 more genes
    nsv7059635inversion1nstd229human GRCh38 chr15: 51,716,761-55,548,818 , GRCh37.p13 chr15: 52,008,958-55,841,016 CCPG1, LOC105370823, 51 more genes
    nsv7059534inversion1nstd229human GRCh38 chr15: 51,726,660-55,605,328 , GRCh37.p13 chr15: 52,018,857-55,897,526 HNRNPA1P74, MYO5C, 50 more genes
    nsv6974313copy number variation1nstd229human GRCh38 chr15: 52,068,601-52,324,700 , GRCh37.p13 chr15: 52,360,798-52,616,897 RPS13P8, LOC112268150, 8 more genes
    nsv6973598copy number variation1nstd229human GRCh38 chr15: 52,155,801-52,460,300 , GRCh37.p13 chr15: 52,447,998-52,752,497 MIR1266, LOC105370819, 5 more genes
    nsv6972144copy number variation1nstd229human GRCh38 chr15: 52,274,493-52,280,920 , GRCh37.p13 chr15: 52,566,690-52,573,117 MIR1266, MYO5C
    nsv6959654copy number variation1nstd229human GRCh38 chr15: 52,233,201-52,283,900 , GRCh37.p13 chr15: 52,525,398-52,576,097 MIR1266, MYO5C
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 PYGO1, RNU6-449P, 125 more genes
    nsv6132897copy number variation1nstd213human GRCh37 chr15: 50,000,000-53,730,001 , GRCh38.p12 chr15: 49,707,803-53,437,804 MAPK6, ARPP19, 65 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4769387copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853 BCL2L10, RNA5SP394, 86 more genes
    nsv4729647copy number variation1nstd102humanUncertain significance GRCh37 chr15: 52,198,882-52,573,715 , GRCh38.p12 chr15: 51,906,685-52,281,518 TMOD3, MIR1266, 13 more genes
    nsv4729282copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 51,792,729-55,134,365 , GRCh38.p12 chr15: 51,500,532-54,842,167 EEF1B2P1, ONECUT1, 41 more genes
    nsv4456655copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,083,229-53,439,931 , GRCh38.p12 chr15: 49,791,032-53,147,734 CERNA1, MAPK6-DT, 64 more genes
    nsv4456196copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352 MIR1266, AQP9, 199 more genes
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