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Items: 1 to 20 of 323

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5944906copy number variation1nstd209human GRCh38 chr16: 399,976-402,433 , GRCh37.p13 chr16: 449,976-452,433 NME4, DECR2
    nsv5933256copy number variation1nstd209human GRCh38 chr16: 399,182-402,153 , GRCh37.p13 chr16: 449,182-452,153 DECR2, NME4
    nsv5867695copy number variation1nstd209human GRCh38 chr16: 400,020-402,512 , GRCh37.p13 chr16: 450,020-452,512 DECR2, NME4
    nsv5660878insertion1nstd207human GRCh38 chr16: 397,716-397,716 , GRCh37.p13 chr16: 447,716-447,716 NME4
    nsv5657588insertion2nstd207human GRCh38 chr16: 397,709-397,709 , GRCh37.p13 chr16: 447,709-447,709 NME4
    nsv5650474insertion1nstd207human GRCh38 chr16: 397,707-397,707 , GRCh37.p13 chr16: 447,707-447,707 NME4
    nsv5526087copy number variation1nstd206human GRCh38 chr16: 399,640-399,735 , GRCh37.p13 chr16: 449,640-449,735 NME4
    nsv5519180copy number variation1nstd206human GRCh38 chr16: 263,125-505,632 , GRCh37.p13 chr16: 313,124-555,632 , ARHGDIG, 11 more genes
    nsv5312899copy number variation1nstd204human GRCh38.p13 chr16: 368,634-401,084 , GRCh37.p13 chr16: 418,634-451,084 , NME4, 5 more genes
    nsv5269885copy number variation1nstd204human GRCh37.p13 chr16: 418,881-450,831 , GRCh38.p13 chr16: 368,881-400,831 , NME4, 5 more genes
    nsv5266479copy number variation1nstd204human GRCh37.p13 chr16: 418,601-451,000 , GRCh38.p13 chr16: 368,601-401,000 , NME4, 5 more genes
    nsv5265522copy number variation1nstd204human GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201 , RHBDL1, 175 more genes
    nsv5145074mobile element insertion1nstd203human GRCh38 chr16: 394,768-394,780 , GRCh37.p13 chr16: 444,768-444,780 , NME4
    nsv5142626mobile element insertion1nstd203human GRCh38 chr16: 394,762-394,762 , GRCh37.p13 chr16: 444,762-444,762 , NME4
    nsv5142418mobile element insertion1nstd203human GRCh38 chr16: 394,763-394,780 , GRCh37.p13 chr16: 444,763-444,780 , NME4
    nsv5009316copy number variation1nstd200human GRCh38 chr16: 401,182-404,897 , GRCh37.p13 chr16: 451,182-454,897 NME4, DECR2
    nsv5009315copy number variation1nstd200human GRCh38 chr16: 393,581-402,352 , GRCh37.p13 chr16: 443,581-452,352 , DECR2, 1 more genes
    nsv5009314copy number variation1nstd200human GRCh38 chr16: 391,303-394,999 , GRCh37.p13 chr16: 441,303-444,999 , LOC100134368, 1 more genes
    nsv5009313copy number variation1nstd200human GRCh38 chr16: 390,815-407,590 , GRCh37.p13 chr16: 440,815-457,590 , NME4, 2 more genes
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