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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904127copy number variation1nstd209human GRCh38 chr3: 9,996,659-11,875,087 , GRCh37.p13 chr3: 10,038,343-11,916,561 , EMC3, 35 more genes
    nsv5901270copy number variation1nstd209human GRCh38 chr3: 10,048,544-11,870,471 , GRCh37.p13 chr3: 10,090,228-11,911,945 , SLC6A11, 29 more genes
    nsv5891525copy number variation1nstd209human GRCh38 chr3: 9,996,478-11,874,953 , GRCh37.p13 chr3: 10,038,162-11,916,427 , TATDN2, 35 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4743065copy number variation1nstd199human GRCh37 chr3: 10,036,258-11,911,948 , GRCh38.p12 chr3: 9,994,574-11,870,474 , ATP2B2-IT2, 36 more genes
    nsv4738819copy number variation1nstd199human GRCh37 chr3: 10,090,229-11,911,947 , GRCh38.p12 chr3: 10,048,545-11,870,473 , LINC00852, 29 more genes
    nsv4679251copy number variation1nstd189human GRCh37.p13 chr3: 10,310,150-10,515,846 , GRCh38.p12 chr3: 10,268,466-10,474,162 ATP2B2, SEC13, 7 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4450300copy number variation1nstd102humanUncertain significance GRCh37 chr3: 10,325,353-10,509,129 , GRCh38.p12 chr3: 10,283,669-10,467,445 GHRLOS, SEC13, 5 more genes
    nsv4435930copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,453,917-12,015,126 , GRCh38.p12 chr3: 9,412,233-11,973,652 VGLL4, JAGN1, 63 more genes
    nsv4322351inversion1nstd166human GRCh37.p13 chr3: 5,153,487-11,332,347 , GRCh38.p12 chr3: 5,111,802-11,290,661 CAV3, HRH1, 96 more genes
    nsv4087204copy number variation1nstd166human GRCh37.p13 chr3: 10,254,945-10,343,951 , GRCh38.p12 chr3: 10,213,261-10,302,267 IRAK2, SEC13, 5 more genes
    nsv3924677copy number variation1nstd102humanPathogenic GRCh38 chr3: 9,875,909-10,572,677 , GRCh37 chr3: 9,917,593-10,614,361 , NCBI36 chr3: 9,892,593-10,589,361 GHRLOS, ATP2B2, 28 more genes
    nsv3924579copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 8,055,414-11,257,617 , GRCh37 chr3: 8,080,414-11,282,617 , GRCh38 chr3: 8,038,727-11,240,931 ATP2B2, CAV3, 74 more genes
    nsv3922069copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 7,992,421-12,653,416 , GRCh37 chr3: 8,017,421-12,678,416 , GRCh38 chr3: 7,975,734-12,636,917 ATP2B2, CAV3, 96 more genes
    nsv3921312copy number variation1nstd102humanUncertain significance NCBI36 chr3: 10,237,646-11,182,135 , GRCh38 chr3: 10,220,962-11,165,449 , GRCh37 chr3: 10,262,646-11,207,135 IRAK2, LINC00606, 17 more genes
    nsv3914273copy number variation1nstd102humanPathogenic NCBI36 chr3: 9,994,160-11,785,084 , GRCh37.p13 chr3: 10,019,160-11,810,084 , GRCh38.p12 chr3: 9,977,476-11,768,610 TAMM41, MIR12127, 34 more genes
    nsv3911723copy number variation1nstd102humanPathogenic GRCh37 chr3: 9,436,558-11,732,086 , GRCh38 chr3: 9,394,874-11,690,612 , NCBI36 chr3: 9,411,558-11,707,086 FANCD2, EMC3, 57 more genes
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