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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
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    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
    nsv5316445copy number variation1nstd204human GRCh38.p13 chr16: 3,034,541-3,068,586 , GRCh37.p13 chr16: 3,084,542-3,118,587 IL32, MMP25, 4 more genes
    nsv5277387copy number variation1nstd204human GRCh38.p13 chr16: 3,034,643-3,038,871 , GRCh37.p13 chr16: 3,084,644-3,088,872 LOC100128770, BICDL2
    nsv5276967copy number variation1nstd204human GRCh38.p13 chr16: 3,037,247-3,045,445 , GRCh37.p13 chr16: 3,087,248-3,095,446 MMP25, BICDL2, 1 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
    nsv5269217copy number variation1nstd204human GRCh37.p13 chr16: 3,084,602-3,118,601 , GRCh38.p13 chr16: 3,034,601-3,068,600 IL32, MMP25, 4 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
    nsv5009365copy number variation1nstd200human GRCh38 chr16: 2,872,374-3,325,224 , GRCh37.p13 chr16: 2,922,375-3,375,224 , ZNF205, 55 more genes
    nsv5007962copy number variation1nstd200human GRCh38 chr16: 2,953,839-3,142,075 , GRCh37.p13 chr16: 3,003,840-3,192,076 , MMP25, 25 more genes
    nsv4866434copy number variation1nstd200human GRCh37 chr16: 3,084,571-3,118,564 , GRCh38.p12 chr16: 3,034,570-3,068,563 IL32, MMP25, 4 more genes
    nsv4866429copy number variation1nstd200human GRCh37 chr16: 2,986,637-3,082,610 , GRCh38.p12 chr16: 2,936,636-3,032,609 , LOC105371055, 14 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
    nsv4667847copy number variation1nstd186human GRCh37 chr16: 3,087,417-3,087,776 , GRCh38.p12 chr16: 3,037,416-3,037,775 BICDL2, LOC100128770
    nsv4629653copy number variation1nstd183human GRCh37 chr16: 2,997,255-3,102,291 , GRCh38.p12 chr16: 2,947,254-3,052,290 , TNFRSF12A, 16 more genes
    nsv4619587copy number variation2nstd183human GRCh37 chr16: 3,087,417-3,087,776 , GRCh38.p12 chr16: 3,037,416-3,037,775 LOC100128770, BICDL2
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