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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7061059inversion1nstd229human GRCh38 chr16: 23,459,969-24,877,943 , GRCh37.p13 chr16: 23,471,290-24,889,264 LOC105371143, CHP2, 20 more genes
    nsv6992469copy number variation1nstd229human GRCh38 chr16: 24,658,141-24,666,226 , GRCh37.p13 chr16: 24,669,462-24,677,547 TNRC6A, LINC01567
    nsv6980511copy number variation1nstd229human GRCh38 chr16: 24,660,097-24,692,873 , GRCh37.p13 chr16: 24,671,418-24,704,194 TNRC6A, LINC01567
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6502818copy number variation1nstd223human GRCh38 chr16: 24,655,464-24,668,189 , GRCh37.p13 chr16: 24,666,785-24,679,510 LINC01567, TNRC6A
    nsv6502053copy number variation1nstd223human GRCh38 chr16: 24,620,908-24,675,425 , GRCh37.p13 chr16: 24,632,229-24,686,746 LINC01567, TNRC6A
    nsv6290289copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981 LOC105371149, SLX1B, 166 more genes
    nsv6289847copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924 GAPDHP35, NSMCE1, 154 more genes
    nsv6234732insertion1nstd214human GRCh38 chr16: 24,664,627-24,664,627 , GRCh37.p13 chr16: 24,675,948-24,675,948 LINC01567, TNRC6A
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
    nsv6133267copy number variation1nstd213human GRCh37 chr16: 22,710,000-30,200,001 , GRCh38.p12 chr16: 22,698,679-30,188,680 ALDOA, AQP8, 169 more genes
    nsv6133266copy number variation1nstd213human GRCh37 chr16: 22,710,000-26,360,001 , GRCh38.p12 chr16: 22,698,679-26,348,680 AQP8, NDUFAB1, 54 more genes
    nsv5976928insertion1nstd209human GRCh38 chr16: 24,664,627-24,664,627 , GRCh37.p13 chr16: 24,675,948-24,675,948 TNRC6A, LINC01567
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5701085mobile element insertion1nstd211human GRCh38 chr16: 24,664,610-24,664,610 , GRCh37.p13 chr16: 24,675,931-24,675,931 LINC01567, TNRC6A
    nsv5531476copy number variation1nstd206human GRCh38 chr16: 24,664,166-24,666,283 , GRCh37.p13 chr16: 24,675,487-24,677,604 LINC01567, TNRC6A
    nsv5141385mobile element insertion1nstd203human GRCh38 chr16: 24,669,941-24,669,968 , GRCh37.p13 chr16: 24,681,262-24,681,289 LINC01567, TNRC6A
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
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