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Items: 1 to 20 of 442

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076319inversion1nstd229human GRCh38 chr8: 58,118,423-58,122,370 , GRCh37.p13 chr8: 59,030,982-59,034,929 FAM110B
    nsv7065739inversion1nstd229human GRCh38 chr8: 58,045,192-58,045,272 , GRCh37.p13 chr8: 58,957,751-58,957,831 FAM110B
    nsv7063355inversion1nstd229human GRCh38 chr8: 58,065,459-58,065,541 , GRCh37.p13 chr8: 58,978,018-58,978,100 FAM110B
    nsv6857897copy number variation1nstd229human GRCh38 chr8: 58,029,118-58,037,418 , GRCh37.p13 chr8: 58,941,677-58,949,977 FAM110B
    nsv6857876copy number variation1nstd229human GRCh38 chr8: 58,113,651-58,132,578 , GRCh37.p13 chr8: 59,026,210-59,045,137 RPL26P26, FAM110B
    nsv6856844copy number variation1nstd229human GRCh38 chr8: 58,031,629-58,318,522 , GRCh37.p13 chr8: 58,944,188-59,231,081 FAM110B, LOC107986945, 2 more genes
    nsv6856393copy number variation1nstd229human GRCh38 chr8: 58,048,159-58,105,523 , GRCh37.p13 chr8: 58,960,718-59,018,082 FAM110B
    nsv6856227copy number variation1nstd229human GRCh38 chr8: 58,041,200-58,059,543 , GRCh37.p13 chr8: 58,953,759-58,972,102 FAM110B
    nsv6855627copy number variation1nstd229human GRCh38 chr8: 58,036,498-58,038,115 , GRCh37.p13 chr8: 58,949,057-58,950,674 FAM110B
    nsv6854956copy number variation1nstd229human GRCh38 chr8: 58,007,811-58,007,851 , GRCh37.p13 chr8: 58,920,370-58,920,410 FAM110B
    nsv6854776copy number variation1nstd229human GRCh38 chr8: 58,034,401-58,036,000 , GRCh37.p13 chr8: 58,946,960-58,948,559 FAM110B
    nsv6852685copy number variation1nstd229human GRCh38 chr8: 58,096,262-58,109,196 , GRCh37.p13 chr8: 59,008,821-59,021,755 FAM110B
    nsv6852143copy number variation1nstd229human GRCh38 chr8: 58,025,353-58,027,855 , GRCh37.p13 chr8: 58,937,912-58,940,414 FAM110B
    nsv6851160copy number variation1nstd229human GRCh38 chr8: 58,035,164-58,039,107 , GRCh37.p13 chr8: 58,947,723-58,951,666 FAM110B
    nsv6849068copy number variation1nstd229human GRCh38 chr8: 58,122,668-58,128,699 , GRCh37.p13 chr8: 59,035,227-59,041,258 FAM110B
    nsv6849045copy number variation1nstd229human GRCh38 chr8: 58,117,458-58,128,631 , GRCh37.p13 chr8: 59,030,017-59,041,190 FAM110B
    nsv6848634copy number variation1nstd229human GRCh38 chr8: 58,117,957-58,122,987 , GRCh37.p13 chr8: 59,030,516-59,035,546 FAM110B
    nsv6847131copy number variation1nstd229human GRCh38 chr8: 58,050,801-58,058,000 , GRCh37.p13 chr8: 58,963,360-58,970,559 FAM110B
    nsv6846670copy number variation1nstd229human GRCh38 chr8: 58,032,655-58,032,836 , GRCh37.p13 chr8: 58,945,214-58,945,395 FAM110B
    nsv6846524copy number variation1nstd229human GRCh38 chr8: 58,102,611-58,111,082 , GRCh37.p13 chr8: 59,015,170-59,023,641 FAM110B
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