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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5928138copy number variation1nstd209human GRCh38 chr16: 15,180,124-18,091,718 , GRCh37.p13 chr16: 15,273,981-18,185,575 , LOC102723692, 42 more genes
    nsv4730208inversion9nstd198human GRCh38 chr16: 16,118,120-18,828,979 , GRCh37.p13 chr16: 16,211,977-18,840,301 , ABCC6, 48 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
    nsv4729488copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,417,030-16,544,419 , GRCh38.p12 chr16: 15,323,173-16,450,562 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,111,619 ABCC6, ABCC1, 26 more genes
    nsv4729445copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,375,911-18,198,455 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 , GRCh38.p12 chr16: 15,282,054-18,104,598 BMERB1, RNU6-213P, 38 more genes
    nsv4729435copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,316,618-18,164,698 , GRCh38.p12 chr16: 15,222,761-18,070,841 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 ABCC6, ABCC1, 37 more genes
    nsv4729194copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,127,985-16,527,476 , GRCh38.p12 chr16: 15,034,128-16,433,619 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,094,665 ABCC6, ABCC1, 37 more genes
    nsv4728965copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,481,920-16,837,613 , GRCh38.p12 chr16: 15,388,063-16,743,756 , GRCh38.p12 chr16|NT_187607.1: 1,046,027-2,404,692 ABCC6, ABCC1, 27 more genes
    nsv4728906copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,481,920-18,164,698 , GRCh38.p12 chr16: 15,388,063-18,070,841 , GRCh38.p12 chr16|NT_187607.1: 1,046,027-2,659,700 ABCC6, ABCC1, 35 more genes
    nsv4728800copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,193,982-18,770,833 , GRCh38.p12 chr16: 15,100,125-18,759,511 ABCC6, ABCC1, 66 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4680237copy number variation1nstd189human GRCh37.p13 chr16: 15,481,935-16,529,591 , GRCh38.p12 chr16: 15,388,078-16,435,734 , GRCh38.p12 chr16|NT_187607.1: 1,046,042-2,096,780 , ABCC6, 26 more genes
    nsv4678926copy number variation1nstd189human GRCh37.p13 chr16: 14,951,417-16,632,977 , GRCh38.p12 chr16: 14,857,560-16,539,120 , ABCC6, 54 more genes
    nsv4676055copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,900,182-16,529,801 , GRCh38.p12 chr16: 14,806,325-16,435,944 ABCC6, ABCC1, 51 more genes
    nsv4675768copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,770,672-16,458,408 , GRCh38.p12 chr16: 14,676,815-16,364,551 RPL15P20, NDE1, 53 more genes
    nsv4675753copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,897,625-16,514,111 , GRCh38.p12 chr16: 14,803,768-16,420,254 MIR6770-1, RNU6-213P, 51 more genes
    nsv4675473copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,900,072-16,837,613 , GRCh38.p12 chr16: 14,806,215-16,743,756 ABCC6, ABCC1, 53 more genes
    nsv4675182copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,481,920-16,516,109 , GRCh38.p12 chr16: 15,388,063-16,422,252 , GRCh38.p12 chr16|NT_187607.1: 1,046,027-2,083,294 ABCC6, ABCC1, 25 more genes
    nsv4675128copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,900,168-16,869,135 , GRCh38.p12 chr16: 14,806,311-16,775,278 ABCC6, ABCC1, 53 more genes
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