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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7060352inversion1nstd229human GRCh38 chr19: 3,851,263-4,364,229 , GRCh37.p13 chr19: 3,851,261-4,364,226 DAPK3, YJU2, 22 more genes
    nsv7012348copy number variation1nstd229human GRCh38 chr19: 4,252,270-4,270,796 , GRCh37.p13 chr19: 4,252,267-4,270,793 YJU2
    nsv7008663copy number variation1nstd229human GRCh38 chr19: 4,247,581-4,247,672 , GRCh37.p13 chr19: 4,247,578-4,247,669 YJU2
    nsv7006298copy number variation1nstd229human GRCh38 chr19: 4,262,454-4,264,775 , GRCh37.p13 chr19: 4,262,451-4,264,772 YJU2
    nsv6624973copy number variation1nstd224human GRCh37 chr19: 4,180,801-4,288,333 , GRCh38.p12 chr19: 4,180,804-4,288,336 EBI3, SIRT6, 3 more genes
    nsv6598603inversion1nstd223human GRCh38 chr19: 4,262,367-4,610,905 , GRCh37.p13 chr19: 4,262,364-4,610,917 STAP2, FSD1, 15 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6525236copy number variation1nstd223human GRCh38 chr19: 4,230,264-4,269,121 , GRCh37.p13 chr19: 4,230,261-4,269,118 EBI3, YJU2
    nsv6521515copy number variation1nstd223human GRCh38 chr19: 4,269,557-4,270,041 , GRCh37.p13 chr19: 4,269,554-4,270,038 YJU2
    nsv6521188copy number variation1nstd223human GRCh38 chr19: 4,266,895-4,287,678 , GRCh37.p13 chr19: 4,266,892-4,287,675 SHD, YJU2
    nsv6521187copy number variation1nstd223human GRCh38 chr19: 4,250,648-4,252,476 , GRCh37.p13 chr19: 4,250,645-4,252,473 YJU2
    nsv6517828copy number variation1nstd223human GRCh38 chr19: 4,255,996-4,257,271 , GRCh37.p13 chr19: 4,255,993-4,257,268 YJU2
    nsv6291587copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,501,624-5,357,124 , GRCh38.p12 chr19: 3,501,626-5,357,113 RN7SL202P, EIF1P6, 67 more genes
    nsv6291557copy number variation1nstd102humanUncertain significance GRCh37 chr19: 4,182,912-4,633,772 , GRCh38.p12 chr19: 4,182,915-4,633,760 STAP2, MIR4746, 19 more genes
    nsv6284296copy number variation1nstd214human GRCh38 chr19: 4,247,621-4,247,671 , GRCh37.p13 chr19: 4,247,618-4,247,668 YJU2
    nsv6280909copy number variation1nstd214human GRCh38 chr19: 4,247,585-4,247,667 , GRCh37.p13 chr19: 4,247,582-4,247,664 YJU2
    nsv6205620copy number variation1nstd214human GRCh38 chr19: 4,247,603-4,247,679 , GRCh37.p13 chr19: 4,247,600-4,247,676 YJU2
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