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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv6987699copy number variation1nstd229human GRCh38 chr16: 67,178,586-67,199,277 , GRCh37.p13 chr16: 67,212,489-67,233,180 MATCAP1, ELMO3, 2 more genes
    nsv6981504copy number variation1nstd229human GRCh38 chr16: 67,202,558-67,205,520 , GRCh37.p13 chr16: 67,236,461-67,239,423 ELMO3, MIR328, 1 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6023823copy number variation1nstd212human GRCh38 chr16: 67,202,558-67,205,520 , GRCh37.p13 chr16: 67,236,461-67,239,423 FBXL9P, ELMO3, 1 more genes
    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
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