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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112816copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,887,031-16,308,753 , GRCh38.p12 chr16: 14,793,174-16,214,896 , GRCh38.p12 chr16|NT_187607.1: 326,909-1,872,893 NTAN1, MIR3179-1, 50 more genes
    nsv6112786copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,124,782-16,291,779 , GRCh38.p12 chr16: 15,030,925-16,197,922 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,855,918 RNU6-213P, LOC105371102, 25 more genes
    nsv5978615insertion1nstd209human GRCh38 chr16: 15,324,335-15,324,335 , GRCh37.p13 chr16: 15,418,192-15,418,192
    nsv5973226insertion1nstd209human GRCh38 chr16: 15,321,997-15,321,997 , GRCh37.p13 chr16: 15,415,854-15,415,854
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5931936copy number variation1nstd209human GRCh38 chr16: 15,318,428-15,321,092 , GRCh37.p13 chr16: 15,412,285-15,414,949
    nsv5928138copy number variation1nstd209human GRCh38 chr16: 15,180,124-18,091,718 , GRCh37.p13 chr16: 15,273,981-18,185,575 , LOC102723692, 42 more genes
    nsv5882493copy number variation2nstd209human GRCh38 chr16: 15,320,657-15,321,973 , GRCh37.p13 chr16: 15,414,514-15,415,830
    nsv5594759copy number variation1nstd207human GRCh38 chr16: 15,322,067-15,322,236 , GRCh37.p13 chr16: 15,415,924-15,416,093
    nsv5544251insertion1nstd206human GRCh38 chr16: 15,324,379-15,324,386 , GRCh37.p13 chr16: 15,418,236-15,418,243
    nsv5528797copy number variation1nstd206human GRCh38 chr16: 15,104,000-15,348,000 , GRCh37.p13 chr16: 15,197,857-15,441,857 , PDXDC1, 8 more genes
    nsv5524190copy number variation1nstd206human GRCh38 chr16: 15,316,000-15,328,000 , GRCh37.p13 chr16: 15,409,857-15,421,857
    nsv5514867copy number variation1nstd206human GRCh38 chr16: 15,302,500-15,328,000 , GRCh37.p13 chr16: 15,396,357-15,421,857
    nsv5514078copy number variation1nstd206human GRCh38 chr16: 15,285,700-15,328,500 , GRCh37.p13 chr16: 15,379,557-15,422,357 , LOC105371097
    nsv5381790copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,126,890-16,293,190 , GRCh38.p12 chr16: 15,033,033-16,199,333 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,857,331 RRN3, CEP20, 25 more genes
    nsv5380983copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,968,859-16,363,239 , GRCh38.p12 chr16: 14,875,002-16,269,382 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,927,385 LOC102724984, LOC728138, 50 more genes
    nsv5279914copy number variation1nstd204human GRCh38.p13 chr16: 15,316,401-15,328,600 , GRCh37.p13 chr16: 15,410,258-15,422,457
    nsv5278329copy number variation1nstd204human GRCh38.p13 chr16: 15,302,501-15,331,700 , GRCh37.p13 chr16: 15,396,358-15,425,557
    nsv5270408copy number variation1nstd204human GRCh38.p13 chr16: 15,321,901-15,322,300 , GRCh37.p13 chr16: 15,415,758-15,416,157
    nsv5265665copy number variation1nstd204human GRCh38.p13 chr16: 15,251,101-15,328,500 , GRCh37.p13 chr16: 15,344,958-15,422,357 , LOC105371097
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