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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5531248copy number variation1nstd206human GRCh38 chr16: 31,177,782-31,178,539 , GRCh37.p13 chr16: 31,189,103-31,189,860 FUS
    nsv5271479copy number variation1nstd204human GRCh38.p13 chr16: 31,177,636-31,180,471 , GRCh37.p13 chr16: 31,188,957-31,191,792 FUS
    nsv5040420inversion1nstd200human GRCh38 chr16: 29,736,418-31,610,189 , GRCh37.p13 chr16: 29,747,739-31,621,510 , ZNF668, 119 more genes
    nsv4879933inversion1nstd200human GRCh37 chr16: 29,747,739-31,621,510 , GRCh38.p12 chr16: 29,736,418-31,610,189 , LOC613038, 119 more genes
    nsv4856841copy number variation1nstd200human GRCh37 chr16: 31,189,102-31,189,815 , GRCh38.p12 chr16: 31,177,781-31,178,494 FUS
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729988copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,350,747-31,905,898 , GRCh38.p12 chr16: 30,339,426-31,894,577 VN1R3, HSD3B7, 89 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4681461copy number variation1nstd102humanUncertain significance GRCh37 chr16: 31,193,709-31,206,202 , GRCh38.p12 chr16: 31,182,388-31,194,881 FUS
    nsv4503085mobile element insertion1nstd166human GRCh37.p13 chr16: 31,203,236-31,203,236 , GRCh38.p12 chr16: 31,191,915-31,191,915 FUS
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4322553inversion1nstd166human GRCh37.p13 chr16: 16,634,964-31,736,102 , GRCh38.p12 chr16: 16,541,107-31,724,781 , ALDOA, 403 more genes
    nsv4239707copy number variation1nstd166human GRCh37.p13 chr16: 31,199,304-31,199,360 , GRCh38.p12 chr16: 31,187,983-31,188,039 FUS
    nsv3924250copy number variation1nstd102humanPathogenic NCBI36 chr16: 29,828,435-31,357,519 , GRCh37 chr16: 29,920,934-31,450,018 , GRCh38 chr16: 29,909,613-31,438,697 MIR4518, ZNF747-DT, 95 more genes
    nsv3918492copy number variation1nstd102humanPathogenic GRCh37 chr16: 30,703,233-35,147,508 , NCBI36 chr16: 30,610,734-35,005,009 , GRCh38 chr16: 30,691,912-36,160,463 KRBOX5P1, LOC110262331, 213 more genes
    nsv3914248copy number variation1nstd102humanPathogenic GRCh37 chr16: 23,763,368-31,955,076 , GRCh38 chr16: 23,752,047-31,943,755 , NCBI36 chr16: 23,670,869-31,862,577 ZG16, TPRKBP2, 250 more genes
    nsv3913895copy number variation1nstd102humanPathogenic NCBI36 chr16: 24,289,454-33,830,560 , GRCh37.p13 chr16: 24,381,953-33,923,059 , GRCh38.p12 chr16: 24,370,632-34,120,592 ITGAL, CORO1A, 310 more genes
    nsv3910351copy number variation1nstd102humanPathogenic GRCh38 chr16: 27,311,746-31,193,406 , NCBI36 chr16: 27,230,568-31,112,228 , GRCh37 chr16: 27,323,067-31,204,727 BCL7C, RNU6-1043P, 171 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 PRSS53, LINC02134, 1868 more genes
    nsv3908692copy number variation1nstd102humanUncertain significance GRCh37 chr16: 31,198,100-31,407,832 , GRCh38.p12 chr16: 31,186,779-31,396,511 PYCARD-AS1, TRIM72, 7 more genes
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