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Items: 1 to 20 of 114

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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
    nsv6992862copy number variation1nstd229human GRCh38 chr16: 67,372,949-67,543,806 , GRCh37.p13 chr16: 67,406,852-67,577,709 AGRP, RNU1-123P, 8 more genes
    nsv6983006copy number variation1nstd229human GRCh38 chr16: 67,480,484-67,496,712 , GRCh37.p13 chr16: 67,514,387-67,530,615 ATP6V0D1-DT, AGRP, 1 more genes
    nsv6503035copy number variation1nstd223human GRCh38 chr16: 67,480,530-67,496,729 , GRCh37.p13 chr16: 67,514,433-67,530,632 AGRP, ATP6V0D1-DT, 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
    nsv5531662copy number variation1nstd206human GRCh38 chr16: 67,473,644-67,491,517 , GRCh37.p13 chr16: 67,507,547-67,525,420 AGRP, ATP6V0D1-DT, 1 more genes
    nsv5524682copy number variation1nstd206human GRCh38 chr16: 67,480,490-67,496,772 , GRCh37.p13 chr16: 67,514,393-67,530,675 AGRP, ATP6V0D1, 1 more genes
    nsv5272913copy number variation1nstd204human GRCh38.p13 chr16: 67,454,801-68,159,500 , GRCh37.p13 chr16: 67,488,704-68,193,403 EDC4, ATP6V0D1, 31 more genes
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    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
    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
    nsv4248859copy number variation1nstd166human GRCh37.p13 chr16: 67,512,900-67,518,000 , GRCh38.p12 chr16: 67,478,997-67,484,097 ATP6V0D1, AGRP, 1 more genes
    nsv4243165copy number variation1nstd166human GRCh37.p13 chr16: 67,514,433-67,530,635 , GRCh38.p12 chr16: 67,480,530-67,496,732 ATP6V0D1, ATP6V0D1-DT, 1 more genes
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