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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074787inversion1nstd229human GRCh38 chr15: 59,615,252-60,468,571 , GRCh37.p13 chr15: 59,907,451-60,760,770 BNIP2, ICE2, 14 more genes
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv7069841inversion1nstd229human GRCh38 chr15: 55,108,583-62,405,114 , GRCh37.p13 chr15: 55,400,781-62,697,313 LOC105370834, RPL21P14, 118 more genes
    nsv6975916copy number variation1nstd229human GRCh38 chr15: 59,894,653-60,113,771 , GRCh37.p13 chr15: 60,186,852-60,405,970 FOXB1, MESTP2, 2 more genes
    nsv6970371copy number variation1nstd229human GRCh38 chr15: 59,749,824-60,113,722 , GRCh37.p13 chr15: 60,042,023-60,405,921 LOC105370838, MESTP2, 4 more genes
    nsv6637744copy number variation1nstd102humanUncertain significance GRCh37 chr15: 60,235,405-60,350,625 , GRCh38.p12 chr15: 59,943,206-60,058,426 LOC105370838, MESTP2, 2 more genes
    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
    nsv6586822inversion1nstd223human GRCh38 chr15: 59,615,251-60,468,567 , GRCh37.p13 chr15: 59,907,450-60,760,766 PIGHP1, MESTP2, 14 more genes
    nsv6133150copy number variation1nstd213human GRCh37 chr15: 59,870,000-66,270,001 , GRCh38.p12 chr15: 59,577,801-65,977,663 GTF2A2, OAZ2, 115 more genes
    nsv6132902copy number variation1nstd213human GRCh37 chr15: 58,580,000-60,640,001 , GRCh38.p12 chr15: 58,287,801-60,347,802 ADAM10, ANXA2, 40 more genes
    nsv6132810copy number variation1nstd213human GRCh37 chr15: 58,540,000-60,640,001 , GRCh38.p12 chr15: 58,247,801-60,347,802 ADAM10, ANXA2, 40 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
    nsv5155800mobile element insertion1nstd203human GRCh38 chr15: 60,007,836-60,007,851 , GRCh37.p13 chr15: 60,300,035-60,300,050 FOXB1
    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
    nsv4675312copy number variation1nstd102humanUncertain significance GRCh37 chr15: 59,592,936-60,360,150 , GRCh38.p12 chr15: 59,300,737-60,067,951 FOXB1, BNIP2, 16 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
    nsv4344078sequence alteration1nstd166human GRCh37.p13 chr15: 59,788,011-60,760,766 , GRCh38.p12 chr15: 59,495,812-60,468,567 , BNIP2, 20 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
    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
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