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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964511insertion1nstd209human GRCh38 chr1: 206,864,617-206,864,617 , GRCh37.p13 chr1: 207,037,962-207,037,962 IL20
    nsv5878499copy number variation1nstd209human GRCh38 chr1: 206,866,197-206,870,667 , GRCh37.p13 chr1: 207,039,542-207,044,012 IL20
    nsv5829171copy number variation1nstd209human GRCh38 chr1: 206,866,225-206,870,627 , GRCh37.p13 chr1: 207,039,570-207,043,972 IL20
    nsv5828869copy number variation1nstd209human GRCh38 chr1: 206,866,125-206,867,324 , GRCh37.p13 chr1: 207,039,470-207,040,669 IL20
    nsv5679389mobile element insertion2nstd211human GRCh38 chr1: 206,864,627-206,864,627 , GRCh37.p13 chr1: 207,037,972-207,037,972 IL20
    nsv5621844insertion1nstd207human GRCh38 chr1: 206,864,617-206,864,617 , GRCh37.p13 chr1: 207,037,962-207,037,962 IL20
    nsv5537288insertion1nstd206human GRCh38 chr1: 206,864,627-206,864,659 , GRCh37.p13 chr1: 207,037,972-207,038,004 IL20
    nsv5441451copy number variation1nstd206human GRCh38 chr1: 206,867,261-206,871,886 , GRCh37.p13 chr1: 207,040,606-207,045,231 IL20
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5354530translocation1nstd200human GRCh38 chr1: 206,871,886-206,871,886 , GRCh38 chr1: 206,867,261-206,867,261 , GRCh37.p13 chr1: 207,040,606-207,040,606 , GRCh37.p13 chr1: 207,045,231-207,045,231 IL20
    nsv5070977mobile element insertion1nstd203human GRCh38 chr1: 206,864,616-206,864,627 , GRCh37.p13 chr1: 207,037,961-207,037,972 IL20
    nsv5068651mobile element insertion1nstd203human GRCh38 chr1: 206,864,617-206,864,627 , GRCh37.p13 chr1: 207,037,962-207,037,972 IL20
    nsv4898379copy number variation1nstd200human GRCh38 chr1: 206,856,529-206,867,470 , GRCh37.p13 chr1: 207,029,874-207,040,815 IL20
    nsv4774141copy number variation1nstd200human GRCh37 chr1: 207,040,606-207,045,231 , GRCh38.p12 chr1: 206,867,261-206,871,886 IL20
    nsv4774140copy number variation1nstd200human GRCh37 chr1: 207,029,874-207,040,815 , GRCh38.p12 chr1: 206,856,529-206,867,470 IL20
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751519insertion1nstd199human GRCh37 chr1: 207,037,970-207,037,970 , GRCh38.p12 chr1: 206,864,625-206,864,625 IL20
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4689804mobile element insertion1nstd186human GRCh37 chr1: 207,037,972-207,037,972 , GRCh38.p12 chr1: 206,864,627-206,864,627 IL20
    nsv4685577copy number variation1nstd102humannot provided GRCh37 chr1: 194,356,425-210,988,710 , GRCh38.p12 chr1: 194,387,295-210,815,368 SEPTIN14P12, LINC02602, 332 more genes
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