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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094558copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,832,402-15,850,391 , GRCh38.p12 chr16: 15,738,545-15,756,534 , GRCh38.p12 chr16|NT_187607.1: 1,396,556-1,414,545 MYH11
    nsv3888133copy number variation1nstd102humanPathogenic GRCh38 chr16: 15,823,235-15,838,272 , GRCh37 chr16: 15,917,092-15,932,129 MYH11
    nsv7094650copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,826,401-15,829,455 , GRCh38.p12 chr16|NT_187607.1: 1,390,555-1,393,609 , GRCh38.p12 chr16: 15,732,544-15,735,598 MYH11
    nsv3879007copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,820,770-15,820,841 , GRCh38 chr16: 15,726,913-15,726,984 MYH11
    nsv7094759copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,892,497-15,892,564 , GRCh38.p12 chr16: 15,798,640-15,798,707 , GRCh38.p12 chr16|NT_187607.1: 1,456,621-1,456,688 MYH11
    nsv3894738copy number variation1nstd102humanBenign GRCh37 chr16: 15,949,951-15,950,250 , GRCh38.p12 chr16|NT_187607.1: 1,514,089-1,514,388 , GRCh38.p12 chr16: 15,856,094-15,856,393 MYH11
    nsv7094758copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,857,633-15,857,768 , GRCh38.p12 chr16: 15,763,776-15,763,911 , GRCh38.p12 chr16|NT_187607.1: 1,421,787-1,421,922 MYH11
    nsv6309993copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,917,092-15,932,109 , GRCh38.p12 chr16: 15,823,235-15,838,252 , GRCh38.p12 chr16|NT_187607.1: 1,481,220-1,496,241 MYH11
    nsv7094813copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,838,966-15,850,391 , GRCh38.p12 chr16: 15,745,109-15,756,534 , GRCh38.p12 chr16|NT_187607.1: 1,403,120-1,414,545 MYH11
    nsv4452323copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,931,755-15,932,119 , GRCh38 chr16: 15,837,898-15,838,262 MYH11
    nsv3889633copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,797,828-15,932,129 , GRCh38 chr16: 15,703,971-15,838,272 MYH11, NDE1
    nsv4451438copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,797,838-15,932,119 , GRCh38 chr16: 15,703,981-15,838,262 MYH11, NDE1
    nsv5980403copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chr16: 15,802,668-15,932,109 , GRCh38.p12 chr16|NT_187607.1: 1,366,822-1,496,241 , GRCh38.p12 chr16: 15,708,811-15,838,252 MYH11, NDE1
    nsv3871665copy number variation2nstd102humanUncertain significance GRCh37 chr16: 15,802,660-15,932,126 , GRCh38 chr16: 15,708,803-15,838,269 MYH11, NDE1
    nsv7094757copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,808,746-15,818,869 , GRCh38.p12 chr16: 15,714,889-15,725,012 , GRCh38.p12 chr16|NT_187607.1: 1,372,900-1,383,023 MYH11, NDE1
    nsv4453110copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,820,685-15,820,931 , GRCh38 chr16: 15,726,828-15,727,074 MYH11, NDE1
    nsv6309845copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,802,658-15,802,708 , GRCh38.p12 chr16: 15,708,801-15,708,851 , GRCh38.p12 chr16|NT_187607.1: 1,366,812-1,366,862 MYH11, NDE1
    nsv5380778copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,795,992-15,951,887 , GRCh38.p12 chr16: 15,702,135-15,858,030 , GRCh38.p12 chr16|NT_187607.1: 1,360,146-1,516,022 MYH11, NDE1
    nsv3877592copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,796,992-15,932,126 , GRCh38 chr16: 15,703,135-15,838,269 MYH11, NDE1
    nsv3886032copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,802,662-15,932,115 , GRCh38 chr16: 15,708,805-15,838,258 MYH11, NDE1
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