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Items: 1 to 20 of 170

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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
    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
    nsv5261097copy number variation1nstd204human GRCh38.p13 chr16: 2,925,201-3,011,800 , GRCh37.p13 chr16: 2,975,202-3,061,801 , CLDN9, 8 more genes
    nsv5009368copy number variation1nstd200human GRCh38 chr16: 2,969,582-2,975,415 , GRCh37.p13 chr16: 3,019,583-3,025,416 PKMYT1, PAQR4
    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
    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
    nsv4629653copy number variation1nstd183human GRCh37 chr16: 2,997,255-3,102,291 , GRCh38.p12 chr16: 2,947,254-3,052,290 , TNFRSF12A, 16 more genes
    nsv4620426copy number variation1nstd183human GRCh37 chr16: 3,016,890-3,017,349 , GRCh38.p12 chr16: 2,966,889-2,967,348 KREMEN2, PAQR4
    nsv4457303copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,716,924-3,055,626 , GRCh38.p12 chr16: 2,666,923-3,005,625 ELOB, PRSS21, 21 more genes
    nsv4456186copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,817,166-3,056,563 , GRCh38.p12 chr16: 2,767,165-3,006,562 PRSS33, SRRM2, 17 more genes
    nsv4455790copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,859,583-3,056,563 , GRCh38.p12 chr16: 2,809,582-3,006,562 KREMEN2, PRSS30P, 12 more genes
    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
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