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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5704253mobile element insertion1nstd211human GRCh38 chr16: 67,531,830-67,531,830 , GRCh37.p13 chr16: 67,565,733-67,565,733 RIPOR1
    nsv5530615copy number variation1nstd206human GRCh38 chr16: 67,531,181-67,534,242 , GRCh37.p13 chr16: 67,565,084-67,568,145 RIPOR1
    nsv5521826copy number variation1nstd206human GRCh38 chr16: 67,519,912-67,523,408 , GRCh37.p13 chr16: 67,553,815-67,557,311 LOC100505942, RIPOR1
    nsv5429825mobile element insertion1nstd206human GRCh38 chr16: 67,531,830-67,531,881 , GRCh37.p13 chr16: 67,565,733-67,565,784 RIPOR1
    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
    nsv4993111copy number variation1nstd200human GRCh38 chr16: 67,530,430-67,545,674 , GRCh37.p13 chr16: 67,564,333-67,579,577 RIPOR1
    nsv4993110copy number variation1nstd200human GRCh38 chr16: 67,518,778-67,520,889 , GRCh37.p13 chr16: 67,552,681-67,554,792 RIPOR1, LOC100505942
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4857480copy number variation1nstd200human GRCh37 chr16: 67,565,084-67,568,145 , GRCh38.p12 chr16: 67,531,181-67,534,242 RIPOR1
    nsv4857479copy number variation1nstd200human GRCh37 chr16: 67,564,333-67,579,577 , GRCh38.p12 chr16: 67,530,430-67,545,674 RIPOR1
    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
    nsv4630893copy number variation2nstd183human GRCh37 chr16: 67,565,133-67,567,676 , GRCh38.p12 chr16: 67,531,230-67,533,773 RIPOR1
    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
    nsv4236844copy number variation1nstd166human GRCh37.p13 chr16: 67,562,852-67,565,631 , GRCh38.p12 chr16: 67,528,949-67,531,728 RIPOR1, LOC100505942
    nsv4232787copy number variation1nstd166human GRCh37.p13 chr16: 67,564,333-67,579,577 , GRCh38.p12 chr16: 67,530,430-67,545,674 RIPOR1
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