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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
    nsv6121579copy number variation1nstd186human GRCh37 chr16: 3,192,267-3,192,363 , GRCh38.p12 chr16: 3,142,266-3,142,362 CASP16P, ZNF213
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5940755copy number variation1nstd209human GRCh38 chr16: 3,146,521-3,146,815 , GRCh37.p13 chr16: 3,196,522-3,196,816 CASP16P
    nsv5932136copy number variation1nstd209human GRCh38 chr16: 3,142,272-3,142,350 , GRCh37.p13 chr16: 3,192,273-3,192,351 CASP16P, ZNF213
    nsv5877085copy number variation1nstd209human GRCh38 chr16: 3,122,639-3,150,671 , GRCh37.p13 chr16: 3,172,640-3,200,672 TRP-AGG6-1, ZNF213, 3 more genes
    nsv5529261copy number variation1nstd206human GRCh38 chr16: 3,142,266-3,142,362 , GRCh37.p13 chr16: 3,192,267-3,192,363 ZNF213, CASP16P
    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
    nsv5264643copy number variation1nstd204human GRCh38.p13 chr16: 2,890,301-3,161,600 , GRCh37.p13 chr16: 2,940,302-3,211,601 , 34 more genes
    nsv5009372copy number variation1nstd200human GRCh38 chr16: 3,143,397-3,147,928 , GRCh37.p13 chr16: 3,193,398-3,197,929 CASP16P
    nsv5009365copy number variation1nstd200human GRCh38 chr16: 2,872,374-3,325,224 , GRCh37.p13 chr16: 2,922,375-3,375,224 , ZNF205, 55 more genes
    nsv4854348copy number variation1nstd200human GRCh37 chr16: 3,193,398-3,197,929 , GRCh38.p12 chr16: 3,143,397-3,147,928 CASP16P
    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
    nsv4631505copy number variation1nstd183human GRCh37 chr16: 3,140,616-3,230,888 , GRCh38.p12 chr16: 3,090,615-3,180,887 TRP-AGG6-1, TRR-CCG1-3, 14 more genes
    nsv4631301copy number variation1nstd183human GRCh37 chr16: 3,140,594-3,232,050 , GRCh38.p12 chr16: 3,090,593-3,182,050 TRP-AGG2-7, ZNF213-AS1, 14 more genes
    nsv4456418copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,112,024-3,738,078 , GRCh38.p12 chr16: 3,062,023-3,688,077 ZNF597, ZNF205-AS1, 55 more genes
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