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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
    nsv5942227copy number variation1nstd209human GRCh38 chr16: 20,650,562-20,650,611 , GRCh37.p13 chr16: 20,661,884-20,661,933 ACSM1
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5871021copy number variation1nstd209human GRCh38 chr16: 20,697,814-20,701,796 , GRCh37.p13 chr16: 20,709,136-20,713,118 ACSM1
    nsv5727704mobile element insertion1nstd211human GRCh38 chr16: 20,655,822-20,655,822 , GRCh37.p13 chr16: 20,667,144-20,667,144 ACSM1
    nsv5711572mobile element insertion2nstd211human GRCh38 chr16: 20,660,889-20,660,889 , GRCh37.p13 chr16: 20,672,211-20,672,211 ACSM1
    nsv5706096mobile element insertion1nstd211human GRCh38 chr16: 20,669,453-20,669,453 , GRCh37.p13 chr16: 20,680,775-20,680,775 ACSM1
    nsv5588474copy number variation1nstd207human GRCh38 chr16: 20,643,735-20,643,800 , GRCh37.p13 chr16: 20,655,057-20,655,122 ACSM1
    nsv5585515copy number variation1nstd207human GRCh38 chr16: 20,679,966-20,680,145 , GRCh37.p13 chr16: 20,691,288-20,691,467 ACSM1
    nsv5559114sequence alteration1nstd206human GRCh38 chr16: 20,698,051-20,701,786 , GRCh37.p13 chr16: 20,709,373-20,713,108 ACSM1
    nsv5558702inversion1nstd206human GRCh38 chr16: 20,654,892-20,657,838 , GRCh37.p13 chr16: 20,666,214-20,669,160 ACSM1
    nsv5529942copy number variation1nstd206human GRCh38 chr16: 20,688,922-20,691,262 , GRCh37.p13 chr16: 20,700,244-20,702,584 ACSM1
    nsv5527697copy number variation1nstd206human GRCh38 chr16: 20,630,395-20,641,804 , GRCh37.p13 chr16: 20,641,717-20,653,126 ACSM1
    nsv5518878copy number variation1nstd206human GRCh38 chr16: 20,698,107-20,701,648 , GRCh37.p13 chr16: 20,709,429-20,712,970 ACSM1
    nsv5517596copy number variation1nstd206human GRCh38 chr16: 20,503,131-20,706,186 , GRCh37.p13 chr16: 20,514,453-20,717,508 , ACSM1, 5 more genes
    nsv5515444copy number variation1nstd206human GRCh38 chr16: 20,671,402-20,671,455 , GRCh37.p13 chr16: 20,682,724-20,682,777 ACSM1
    nsv5417876mobile element insertion1nstd206human GRCh38 chr16: 20,660,889-20,660,940 , GRCh37.p13 chr16: 20,672,211-20,672,262 ACSM1
    nsv5365544translocation1nstd200human GRCh38 chr16: 20,650,678-20,650,678 , GRCh38 chr16: 20,652,290-20,652,290 , GRCh37.p13 chr16: 20,662,000-20,662,000 , GRCh37.p13 chr16: 20,663,612-20,663,612 ACSM1
    nsv5303829copy number variation1nstd204human GRCh38.p13 chr16: 20,688,043-20,697,769 , GRCh37.p13 chr16: 20,699,365-20,709,091 ACSM1
    nsv5266434copy number variation1nstd204human GRCh38.p13 chr16: 20,604,661-20,648,186 , GRCh37.p13 chr16: 20,615,983-20,659,508 ACSM5P1, ACSM1, 1 more genes
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