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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5703912mobile element insertion1nstd211human GRCh38 chr16: 67,198,847-67,198,847 , GRCh37.p13 chr16: 67,232,750-67,232,750 E2F4, ELMO3
    nsv5416053mobile element insertion1nstd206human GRCh38 chr16: 67,198,847-67,198,898 , GRCh37.p13 chr16: 67,232,750-67,232,801 ELMO3, E2F4
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005781copy number variation1nstd200human GRCh38 chr16: 67,178,586-67,199,277 , GRCh37.p13 chr16: 67,212,489-67,233,180 MATCAP1, ELMO3, 2 more genes
    nsv5005780copy number variation1nstd200human GRCh38 chr16: 67,159,261-67,221,610 , GRCh37.p13 chr16: 67,193,164-67,255,513 TRADD, HSF4, 8 more genes
    nsv5005779copy number variation1nstd200human GRCh38 chr16: 67,159,176-67,212,734 , GRCh37.p13 chr16: 67,193,079-67,246,637 EXOC3L1, FBXL9P, 8 more genes
    nsv4993093copy number variation1nstd200human GRCh38 chr16: 67,202,558-67,205,520 , GRCh37.p13 chr16: 67,236,461-67,239,423 ELMO3, FBXL9P, 1 more genes
    nsv4993092copy number variation1nstd200human GRCh38 chr16: 67,199,013-67,199,079 , GRCh37.p13 chr16: 67,232,916-67,232,982 ELMO3, E2F4
    nsv4993091copy number variation1nstd200human GRCh38 chr16: 67,198,383-67,198,514 , GRCh37.p13 chr16: 67,232,286-67,232,417 E2F4, ELMO3
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4675201copy number variation1nstd102humanPathogenic GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280 LOC100420066, LINC00920, 143 more genes
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4423203copy number variation1nstd174human GRCh37 chr16: 67,175,101-67,323,199 , GRCh38.p12 chr16: 67,141,198-67,289,296 EXOC3L1, MIR328, 15 more genes
    nsv4350223copy number variation1nstd102humanPathogenic GRCh37 chr16: 67,132,790-68,166,320 , GRCh38.p12 chr16: 67,098,887-68,132,417 CBFB, B3GNT9, 55 more genes
    nsv4332560sequence alteration1nstd166human GRCh37.p13 chr16: 57,901,049-75,540,778 , GRCh38.p12 chr16: 57,867,145-75,506,880 , AGRP, 331 more genes
    nsv4237842copy number variation1nstd166human GRCh37.p13 chr16: 67,236,461-67,239,423 , GRCh38.p12 chr16: 67,202,558-67,205,520 FBXL9P, ELMO3, 1 more genes
    nsv3924078copy number variation1nstd102humanUncertain significance NCBI36 chr16: 65,484,671-66,350,189 , GRCh37.p13 chr16: 66,927,170-67,792,688 , GRCh38.p12 chr16: 66,893,267-67,758,785 ENKD1, LOC100505942, 45 more genes
    nsv3923741copy number variation1nstd102humanUncertain significance GRCh37 chr16: 66,927,107-67,391,081 , GRCh38 chr16: 66,893,204-67,357,178 , NCBI36 chr16: 65,484,608-65,948,582 CIAO2B, EXOC3L1, 27 more genes
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