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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7064795inversion1nstd229human GRCh38 chr16: 2,949,168-3,031,021 , GRCh37.p13 chr16: 2,999,169-3,081,022 CLDN6, PAQR4, 11 more genes
    nsv6972853copy number variation1nstd229human GRCh38 chr16: 2,953,839-3,142,079 , GRCh37.p13 chr16: 3,003,840-3,192,080 TNFRSF12A, LOC100128770, 21 more genes
    nsv6972133copy number variation1nstd229human GRCh38 chr16: 2,909,491-3,033,519 , GRCh37.p13 chr16: 2,959,492-3,083,520 RPL23AP86, PKMYT1, 12 more genes
    nsv6970220copy number variation1nstd229human GRCh38 chr16: 2,974,406-3,077,487 , GRCh37.p13 chr16: 3,024,407-3,127,488 TNFRSF12A, CLDN9, 12 more genes
    nsv6969808copy number variation1nstd229human GRCh38 chr16: 2,947,095-3,056,638 , GRCh37.p13 chr16: 2,997,096-3,106,639 KREMEN2, LOC105371055, 13 more genes
    nsv6969791copy number variation1nstd229human GRCh38 chr16: 2,939,852-3,079,791 , GRCh37.p13 chr16: 2,989,853-3,129,792 MMP25-AS1, RNU1-125P, 16 more genes
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6509277copy number variation1nstd223human GRCh38 chr16: 2,909,491-3,033,519 , GRCh37.p13 chr16: 2,959,492-3,083,520 TNFRSF12A, THOC6, 12 more genes
    nsv6504080copy number variation1nstd223human GRCh38 chr16: 3,011,639-3,016,951 , GRCh37.p13 chr16: 3,061,640-3,066,952 CLDN6, CLDN9
    nsv6290044copy number variation1nstd218human GRCh38.p12 chr16: 2,757,479-3,781,321 , GRCh37 chr16: 2,807,480-3,831,322 , CREBBP, 87 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6133274copy number variation1nstd213human GRCh37 chr16: 2,660,000-3,710,001 , GRCh38.p12 chr16: 2,609,999-3,660,000 DNASE1, MEFV, 90 more genes
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv6093891insertion1nstd212human GRCh38 chr16: 3,016,284-3,016,284 , GRCh37.p13 chr16: 3,066,285-3,066,285 CLDN6
    nsv5517451copy number variation1nstd206human GRCh38 chr16: 3,016,349-3,065,688 , GRCh37.p13 chr16: 3,066,350-3,115,689 CLDN6, IL32, 7 more genes
    nsv5272285copy number variation1nstd204human GRCh38.p13 chr16: 2,651,201-3,235,500 , GRCh37.p13 chr16: 2,701,202-3,285,500 , RNU1-125P, 64 more genes
    nsv5269318copy number variation1nstd204human GRCh38.p13 chr16: 1,733,301-3,469,700 , GRCh37.p13 chr16: 1,783,302-3,519,700 , MIR6511B1, 156 more genes
    nsv5264643copy number variation1nstd204human GRCh38.p13 chr16: 2,890,301-3,161,600 , GRCh37.p13 chr16: 2,940,302-3,211,601 , 34 more genes
    nsv5141839mobile element insertion1nstd203human GRCh38 chr16: 3,016,821-3,016,832 , GRCh37.p13 chr16: 3,066,822-3,066,833 CLDN6
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