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Items: 1 to 20 of 273

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5870602copy number variation1nstd209human GRCh38 chr1: 118,939,575-118,940,995 , GRCh37.p13 chr1: 119,482,198-119,483,618 TBX15
    nsv5827825copy number variation1nstd209human GRCh38 chr1: 118,939,523-118,941,022 , GRCh37.p13 chr1: 119,482,146-119,483,645 TBX15
    nsv5674580mobile element insertion1nstd211human GRCh38 chr1: 118,955,197-118,955,197 , GRCh37.p13 chr1: 119,497,820-119,497,820 TBX15
    nsv5567898copy number variation1nstd207human GRCh38 chr1: 118,939,575-118,940,995 , GRCh37.p13 chr1: 119,482,198-119,483,618 TBX15
    nsv5563919sequence alteration1nstd206human GRCh38 chr1: 118,949,839-118,951,137 , GRCh37.p13 chr1: 119,492,462-119,493,760 TBX15
    nsv5541730insertion1nstd206human GRCh38 chr1: 118,949,840-118,949,840 , GRCh37.p13 chr1: 119,492,463-119,492,463 TBX15
    nsv5414113copy number variation1nstd206human GRCh38 chr1: 118,939,578-118,940,996 , GRCh37.p13 chr1: 119,482,201-119,483,619 TBX15
    nsv5409810mobile element insertion1nstd206human GRCh38 chr1: 118,955,197-118,955,248 , GRCh37.p13 chr1: 119,497,820-119,497,871 TBX15
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5289100copy number variation1nstd204human GRCh38.p13 chr1: 118,939,548-118,941,024 , GRCh37.p13 chr1: 119,482,171-119,483,647 TBX15
    nsv5066921mobile element insertion1nstd203human GRCh38 chr1: 118,939,407-118,939,442 , GRCh37.p13 chr1: 119,482,030-119,482,065 TBX15
    nsv4891004copy number variation1nstd200human GRCh38 chr1: 118,939,578-118,940,996 , GRCh37.p13 chr1: 119,482,201-119,483,619 TBX15
    nsv4773856copy number variation1nstd200human GRCh37 chr1: 119,482,201-119,483,619 , GRCh38.p12 chr1: 118,939,578-118,940,996 TBX15
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4745469copy number variation1nstd199human GRCh37 chr1: 86,005,697-146,486,085 , GRCh38.p12 chr1: 85,540,014-149,528,945 , TAF13, 920 more genes
    nsv4728239copy number variation1nstd102humanUncertain significance GRCh37 chr1: 119,188,808-119,632,855 , GRCh38.p12 chr1: 118,646,185-119,090,232 WARS2-IT1, WARS2, 5 more genes
    nsv4665119copy number variation1nstd186human GRCh37 chr1: 119,482,198-119,483,619 , GRCh38.p12 chr1: 118,939,575-118,940,996 TBX15
    nsv4660716copy number variation1nstd186human GRCh37 chr1: 119,482,482-119,483,626 , GRCh38.p12 chr1: 118,939,859-118,941,003 TBX15
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