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Items: 1 to 20 of 26

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3870498copy number variation1nstd102humanBenign GRCh37 chr3: 37,979,059-37,996,268 , GRCh38.p12 chr3: 37,937,568-37,954,777 CTDSPL
    nsv3877086copy number variation1nstd102humanBenign GRCh37 chr3: 37,973,595-37,990,100 , GRCh38.p12 chr3: 37,932,104-37,948,609 CTDSPL
    nsv3878714copy number variation1nstd102humanBenign GRCh37 chr3: 37,979,059-37,990,100 , GRCh38.p12 chr3: 37,937,568-37,948,609 CTDSPL
    nsv5673469copy number variation3nstd102humannot provided GRCh38 chr3: 37,938,390-37,944,757 , GRCh37 chr3: 37,979,881-37,986,248 CTDSPL
    esv3648682copy number variation1estd216humannot provided GRCh37 chr3: 37,979,882-37,986,249 , GRCh38.p12 chr3: 37,938,391-37,944,758 CTDSPL
    esv3648659copy number variation1estd216humannot provided GRCh37 chr3: 37,979,882-37,986,249 , GRCh38.p12 chr3: 37,938,391-37,944,758 CTDSPL
    esv3648637copy number variation1estd216humannot provided GRCh37 chr3: 37,979,882-37,986,249 , GRCh38.p12 chr3: 37,938,391-37,944,758 CTDSPL
    nsv3883283copy number variation1nstd102humanBenign GRCh37 chr3: 37,979,059-38,009,700 , GRCh38.p12 chr3: 37,937,568-37,968,209 CTDSPL, MIR26A1
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 CTDSPL, LOC102724104, 291 more genes
    nsv4453595copy number variation1nstd102humanPathogenic GRCh37 chr3: 37,493,856-38,991,863 , GRCh38 chr3: 37,452,365-38,950,372 CTDSPL, DLEC1P1, 30 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 CTDSPL, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 CTDSPL, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 CTDSPL, RPL23AP49, 2875 more genes
    nsv3905127copy number variation1nstd102humanPathogenic GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521 CTDSPL, LINC02022, 540 more genes
    nsv3885169copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431 CTDSPL, RNU6-243P, 382 more genes
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 CTDSPL, RN7SL4P, 348 more genes
    nsv3917642copy number variation1nstd102humanPathogenic NCBI36 chr3: 33,744,902-40,678,946 , GRCh37 chr3: 33,769,898-40,703,942 , GRCh38 chr3: 33,728,406-40,662,451 CTDSPL, STAC, 111 more genes
    nsv3883164copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787 CTDSPL, ACAA1, 344 more genes
    nsv3872215copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,493,846-38,991,873 , GRCh38.p12 chr3: 37,452,355-38,950,382 CTDSPL, ITGA9-AS1, 30 more genes
    nsv4674307copy number variation1nstd102humanUncertain significance GRCh37 chr3: 37,987,092-38,194,369 , GRCh38.p12 chr3: 37,945,601-38,152,878 CTDSPL, PLCD1, 7 more genes
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