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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6977204copy number variation1nstd229human GRCh38 chr15: 59,114,701-59,207,600 , GRCh37.p13 chr15: 59,406,900-59,499,799 CCNB2, LDHAL6B, 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
    nsv6622915copy number variation1nstd224human GRCh37 chr15: 59,464,117-59,646,991 , GRCh38.p12 chr15: 59,171,918-59,354,792 RNU4-80P, LDHAL6B, 2 more genes
    nsv6506305copy number variation1nstd223human GRCh38 chr15: 59,203,501-59,205,200 , GRCh37.p13 chr15: 59,495,700-59,497,399 LDHAL6B, MYO1E
    nsv6314097copy number variation1nstd102humanUncertain significance GRCh37 chr15: 59,384,216-59,530,214 , GRCh38.p12 chr15: 59,092,017-59,238,015 CCNB2, LDHAL6B, 4 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
    nsv5561109sequence alteration1nstd206human GRCh38 chr15: 58,869,604-59,552,865 , GRCh37.p13 chr15: 59,161,803-59,845,064 MYO1E, RNF111, 14 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
    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
    nsv4381633copy number variation1nstd173human GRCh37 chr15: 59,486,917-59,515,104 , GRCh38.p12 chr15: 59,194,718-59,222,905 RNU4-80P, MYO1E, 1 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
    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
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