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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5561109sequence alteration1nstd206human GRCh38 chr15: 58,869,604-59,552,865 , GRCh37.p13 chr15: 59,161,803-59,845,064 MYO1E, RNF111, 14 more genes
    nsv5527743copy number variation1nstd206human GRCh38 chr15: 59,109,990-59,112,962 , GRCh37.p13 chr15: 59,402,189-59,405,161 CCNB2
    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
    nsv5183212mobile element insertion1nstd203human GRCh38 chr15: 59,121,447-59,121,464 , GRCh37.p13 chr15: 59,413,646-59,413,663 CCNB2
    nsv5158918mobile element insertion1nstd203human GRCh38 chr15: 59,122,266-59,122,310 , GRCh37.p13 chr15: 59,414,465-59,414,509 CCNB2
    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
    nsv4631336copy number variation1nstd183human GRCh37 chr15: 59,392,246-59,399,923 , GRCh38.p12 chr15: 59,100,047-59,107,724 CCNB2
    nsv4626454copy number variation1nstd183human GRCh37 chr15: 59,388,607-59,399,923 , GRCh38.p12 chr15: 59,096,408-59,107,724 RNF111, CCNB2
    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
    nsv4368274copy number variation1nstd173human GRCh37 chr15: 57,859,275-59,410,122 , GRCh38.p12 chr15: 57,567,077-59,117,923 , RPL28P4, 28 more genes
    nsv4319151inversion1nstd166human GRCh37.p13 chr15: 58,916,342-60,310,178 , GRCh38.p12 chr15: 58,624,143-60,017,979 , MYO1E, 35 more genes
    nsv3948983insertion1nstd167human GRCh37 chr15: 59,408,734-59,408,734 , GRCh38.p12 chr15: 59,116,535-59,116,535 CCNB2
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3921425copy number variation1nstd102humanPathogenic NCBI36 chr15: 55,647,440-61,098,667 , GRCh37 chr15: 57,860,148-63,311,614 , GRCh38 chr15: 57,567,950-63,019,415 MESTP2, HMGB1P51, 86 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 more genes
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