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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121464copy number variation1nstd186human GRCh37 chr16: 3,263,279-3,263,572 , GRCh38.p12 chr16: 3,213,279-3,213,572 OR1F2P
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5594057copy number variation1nstd207human GRCh38 chr16: 3,213,277-3,213,571 , GRCh37.p13 chr16: 3,263,277-3,263,571 OR1F2P
    nsv5524753copy number variation1nstd206human GRCh38 chr16: 3,213,277-3,213,572 , GRCh37.p13 chr16: 3,263,277-3,263,572 OR1F2P
    nsv5521358copy number variation1nstd206human GRCh38 chr16: 3,208,003-3,350,991 , GRCh37.p13 chr16: 3,258,003-3,400,991 MEFV, ZNF75A, 6 more genes
    nsv5315966copy number variation1nstd204human GRCh38.p13 chr16: 3,206,158-3,270,359 , GRCh37.p13 chr16: 3,256,158-3,320,359 OR1F1, ZNF200, 3 more genes
    nsv5280095copy number variation1nstd204human GRCh38.p13 chr16: 3,215,925-3,217,424 , GRCh37.p13 chr16: 3,265,925-3,267,424 OR1F2P
    nsv5280011copy number variation1nstd204human GRCh38.p13 chr16: 3,205,932-3,246,558 , GRCh37.p13 chr16: 3,255,932-3,296,558 OR1F2P, MEFV, 2 more genes
    nsv5277469copy number variation1nstd204human GRCh38.p13 chr16: 3,195,501-3,246,600 , GRCh37.p13 chr16: 3,245,501-3,296,600 TRK-CTT14-1, MEFV, 3 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
    nsv5009379copy number variation1nstd200human GRCh38 chr16: 3,206,166-3,270,351 , GRCh37.p13 chr16: 3,256,166-3,320,351 OR1F1, ZNF200, 3 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
    nsv5007991copy number variation1nstd200human GRCh38 chr16: 3,211,081-3,219,549 , GRCh37.p13 chr16: 3,261,081-3,269,549 OR1F2P
    nsv5007989copy number variation1nstd200human GRCh38 chr16: 3,208,468-3,215,339 , GRCh37.p13 chr16: 3,258,468-3,265,339 OR1F2P
    nsv4866451copy number variation1nstd200human GRCh37 chr16: 3,261,081-3,269,549 , GRCh38.p12 chr16: 3,211,081-3,219,549 OR1F2P
    nsv4866449copy number variation1nstd200human GRCh37 chr16: 3,258,468-3,265,335 , GRCh38.p12 chr16: 3,208,468-3,215,335 OR1F2P
    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
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