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Items: 1 to 20 of 152

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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
    nsv7077695inversion1nstd229human GRCh38 chr16: 2,815,616-2,880,847 , GRCh37.p13 chr16: 2,865,617-2,930,848 PRSS21, ZG16B, 5 more genes
    nsv6975973copy number variation1nstd229human GRCh38 chr16: 2,831,488-2,837,879 , GRCh37.p13 chr16: 2,881,489-2,887,880 ZG16B, PRSS30P
    nsv6969027copy number variation1nstd229human GRCh38 chr16: 2,813,867-2,860,687 , GRCh37.p13 chr16: 2,863,868-2,910,688 PRSS30P, EIF1P4, 3 more genes
    nsv6966239copy number variation1nstd229human GRCh38 chr16: 2,820,272-2,998,796 , GRCh37.p13 chr16: 2,870,273-3,048,797 ZG16B, KREMEN2, 12 more genes
    nsv6965259copy number variation1nstd229human GRCh38 chr16: 2,832,041-2,841,677 , GRCh37.p13 chr16: 2,882,042-2,891,678 PRSS30P, ZG16B
    nsv6637409copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,794,763-2,993,610 , GRCh38.p12 chr16: 2,744,762-2,943,609 RPL23AP86, FLYWCH1, 14 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
    nsv6503727copy number variation1nstd223human GRCh38 chr16: 2,832,040-2,841,677 , GRCh37.p13 chr16: 2,882,041-2,891,678 PRSS30P, ZG16B
    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
    nsv6133194copy number variation1nstd213human GRCh37 chr16: 2,800,000-2,970,001 , GRCh38.p12 chr16: 2,749,999-2,920,000 ELOB, PRSS21, 12 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
    nsv6030544copy number variation1nstd212human GRCh38 chr16: 2,834,665-2,940,872 , GRCh37.p13 chr16: 2,884,666-2,990,873 PRSS22, FLYWCH1, 5 more genes
    nsv5529678copy number variation1nstd206human GRCh38 chr16: 2,837,597-2,837,707 , GRCh37.p13 chr16: 2,887,598-2,887,708 PRSS30P
    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
    nsv5262390copy number variation1nstd204human GRCh38.p13 chr16: 2,578,401-2,889,000 , GRCh37.p13 chr16: 2,628,402-2,939,001 PRSS30P, ELOB, 18 more genes
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
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