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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5929857copy number variation1nstd209human GRCh38 chr16: 3,161,556-3,195,361 , GRCh37.p13 chr16: 3,211,557-3,245,361 TRP-CGG1-2, TRK-CTT2-5, 11 more genes
    nsv5526003copy number variation1nstd206human GRCh38 chr16: 3,179,169-3,199,032 , GRCh37.p13 chr16: 3,229,170-3,249,032 TRP-AGG2-8, TRR-CCT5-1, 8 more genes
    nsv5516459copy number variation1nstd206human GRCh38 chr16: 3,161,556-3,195,364 , GRCh37.p13 chr16: 3,211,557-3,245,364 TRP-TGG4-1, TRK-CTT4-1, 11 more genes
    nsv5304692copy number variation1nstd204human GRCh38.p13 chr16: 3,161,552-3,195,366 , GRCh37.p13 chr16: 3,211,553-3,245,366 TRK-CTT14-1, TRP-TGG3-5, 11 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
    nsv5267763copy number variation1nstd204human GRCh38.p13 chr16: 3,042,701-3,196,700 , GRCh37.p13 chr16: 3,092,702-3,246,700 , OR1F1, 29 more genes
    nsv5267616copy number variation1nstd204human GRCh38.p13 chr16: 3,163,201-3,195,400 , GRCh37.p13 chr16: 3,213,202-3,245,400 TRP-AGG2-8, TRP-AGG2-7, 11 more genes
    nsv5265005copy number variation1nstd204human GRCh38.p13 chr16: 3,160,195-3,194,533 , GRCh37.p13 chr16: 3,210,196-3,244,533 OR1F1, TRP-TGG3-4, 11 more genes
    nsv5009377copy number variation1nstd200human GRCh38 chr16: 3,175,620-3,191,647 , GRCh37.p13 chr16: 3,225,621-3,241,647 OR1F1, TRK-CTT4-1, 7 more genes
    nsv5009376copy number variation1nstd200human GRCh38 chr16: 3,161,556-3,195,364 , GRCh37.p13 chr16: 3,211,557-3,245,364 TRP-AGG2-7, TRP-TGG3-4, 11 more genes
    nsv5009365copy number variation1nstd200human GRCh38 chr16: 2,872,374-3,325,224 , GRCh37.p13 chr16: 2,922,375-3,375,224 , ZNF205, 55 more genes
    nsv5007986copy number variation1nstd200human GRCh38 chr16: 3,192,115-3,196,892 , GRCh37.p13 chr16: 3,242,115-3,246,892 TRK-CTT14-1, TRP-AGG1-1, 2 more genes
    nsv4854343copy number variation1nstd200human GRCh37 chr16: 2,922,375-3,375,224 , GRCh38.p12 chr16: 2,872,374-3,325,224 , RNU1-125P, 55 more genes
    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
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4675826copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,651,354-4,614,965 , GRCh38.p12 chr16: 2,601,353-4,564,964 MEFV, TRR-CCT5-1, 111 more genes
    nsv4626298copy number variation1nstd183human GRCh37 chr16: 3,200,596-3,249,363 , GRCh38.p12 chr16: 3,150,595-3,199,363 OR1F1, TRK-CTT2-5, 16 more genes
    nsv4620801copy number variation1nstd183human GRCh37 chr16: 3,215,287-3,241,444 , GRCh38.p12 chr16: 3,165,286-3,191,444 TRK-CTT5-1, TRP-AGG1-1, 9 more genes
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