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Items: 1 to 20 of 218

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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
    nsv5889306copy number variation1nstd209human GRCh38 chr3: 10,250,265-10,250,437 , GRCh37.p13 chr3: 10,291,949-10,292,121 TATDN2
    nsv5549103insertion1nstd206human GRCh38 chr3: 10,274,764-10,274,801 , GRCh37.p13 chr3: 10,316,448-10,316,485 TATDN2
    nsv5451222copy number variation1nstd206human GRCh38 chr3: 10,258,015-10,258,127 , GRCh37.p13 chr3: 10,299,699-10,299,811 TATDN2
    nsv5078040mobile element insertion1nstd203human GRCh38 chr3: 10,271,956-10,271,956 , GRCh37.p13 chr3: 10,313,640-10,313,640 TATDN2
    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
    nsv4924175copy number variation1nstd200human GRCh38 chr3: 10,250,265-10,250,438 , GRCh37.p13 chr3: 10,291,949-10,292,122 TATDN2
    nsv4917740copy number variation1nstd200human GRCh38 chr3: 10,264,961-10,267,172 , GRCh37.p13 chr3: 10,306,645-10,308,856 TATDN2
    nsv4917739copy number variation1nstd200human GRCh38 chr3: 10,252,867-10,257,664 , GRCh37.p13 chr3: 10,294,551-10,299,348 TATDN2
    nsv4917738copy number variation1nstd200human GRCh38 chr3: 10,252,921-10,255,045 , GRCh37.p13 chr3: 10,294,605-10,296,729 TATDN2
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4796288copy number variation1nstd200human GRCh37 chr3: 10,294,605-10,296,729 , GRCh38.p12 chr3: 10,252,921-10,255,045 TATDN2
    nsv4793842copy number variation1nstd200human GRCh37 chr3: 10,291,949-10,292,122 , GRCh38.p12 chr3: 10,250,265-10,250,438 TATDN2
    nsv4787085mobile element deletion1nstd200human GRCh37 chr3: 10,294,545-10,294,838 , GRCh38.p12 chr3: 10,252,861-10,253,154 TATDN2
    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
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