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Items: 1 to 20 of 174

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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
    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
    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
    nsv5007966copy number variation1nstd200human GRCh38 chr16: 3,019,932-3,020,060 , GRCh37.p13 chr16: 3,069,933-3,070,061 TNFRSF12A
    nsv5007962copy number variation1nstd200human GRCh38 chr16: 2,953,839-3,142,075 , GRCh37.p13 chr16: 3,003,840-3,192,076 , MMP25, 25 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
    nsv4854345copy number variation1nstd200human GRCh37 chr16: 3,069,222-3,075,185 , GRCh38.p12 chr16: 3,019,221-3,025,184 THOC6, TNFRSF12A, 1 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
    nsv4629653copy number variation1nstd183human GRCh37 chr16: 2,997,255-3,102,291 , GRCh38.p12 chr16: 2,947,254-3,052,290 , TNFRSF12A, 16 more genes
    nsv4619615copy number variation2nstd183human GRCh37 chr16: 3,071,503-3,071,614 , GRCh38.p12 chr16: 3,021,502-3,021,613 HCFC1R1, TNFRSF12A
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4365040copy number variation1nstd173human GRCh37 chr16: 2,805,634-3,224,098 , GRCh38.p12 chr16: 2,755,633-3,174,097 , TRR-CCT3-1, 48 more genes
    nsv4349832copy number variation1nstd102humanPathogenic GRCh37 chr16: 109,978-4,316,797 , GRCh38.p12 chr16: 59,980-4,266,796 LINC00235, RNF151, 269 more genes
    nsv4242705copy number variation1nstd166human GRCh37.p13 chr16: 3,066,815-3,069,295 , GRCh38.p12 chr16: 3,016,814-3,019,294 TNFRSF12A, CLDN6
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