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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076096inversion1nstd229human GRCh38 chr21: 32,169,949-32,169,969 , GRCh37.p13 chr21: 33,542,261-33,542,281 MIS18A
    nsv7070554inversion1nstd229human GRCh38 chr21: 28,138,154-35,660,050 , GRCh37.p13 chr21: 29,510,473-37,032,348 , OR7E23P, 160 more genes
    nsv7070253inversion1nstd229human GRCh38 chr21: 28,377,443-35,730,342 , GRCh37.p13 chr21: 29,749,764-37,102,640 , HUNK, 161 more genes
    nsv7067783inversion1nstd229human GRCh38 chr21: 32,166,189-32,171,967 , GRCh37.p13 chr21: 33,538,501-33,544,279 MIS18A
    nsv7066273inversion1nstd229human GRCh38 chr21: 31,423,658-33,221,331 , GRCh37.p13 chr21: 32,795,971-34,593,636 MRAP, FBXW11P1, 37 more genes
    nsv7066036inversion1nstd229human GRCh38 chr21: 29,840,839-33,329,795 , GRCh37.p13 chr21: 31,213,156-34,702,101 SYNJ1, CLDN8, 95 more genes
    nsv7062791inversion1nstd229human GRCh38 chr21: 32,139,318-32,171,975 , GRCh37.p13 chr21: 33,511,629-33,544,287 MIS18A
    nsv7061715inversion1nstd229human GRCh38 chr21: 32,142,918-32,174,798 , GRCh37.p13 chr21: 33,515,229-33,547,110 MIS18A
    nsv7037204copy number variation1nstd229human GRCh38 chr21: 32,228,543-32,231,926 , GRCh37.p13 chr21: 33,600,855-33,604,238 MIS18A
    nsv7036389copy number variation1nstd229human GRCh38 chr21: 31,901,603-32,375,032 , GRCh37.p13 chr21: 33,273,915-33,747,341 MIS18A, MRAP, 4 more genes
    nsv7035959copy number variation1nstd229human GRCh38 chr21: 32,180,487-32,200,178 , GRCh37.p13 chr21: 33,552,799-33,572,490 MIS18A
    nsv7035645copy number variation1nstd229human GRCh38 chr21: 32,232,083-32,234,489 , GRCh37.p13 chr21: 33,604,395-33,606,801 MIS18A
    nsv7034594copy number variation1nstd229human GRCh38 chr21: 32,135,548-32,154,003 , GRCh37.p13 chr21: 33,507,859-33,526,315 MIS18A
    nsv7034332copy number variation1nstd229human GRCh38 chr21: 32,178,102-32,181,549 , GRCh37.p13 chr21: 33,550,414-33,553,861 MIS18A
    nsv7034312copy number variation1nstd229human GRCh38 chr21: 32,035,474-32,170,740 , GRCh37.p13 chr21: 33,407,787-33,543,052 LINC00159, MIS18A
    nsv7033803copy number variation1nstd229human GRCh38 chr21: 32,245,801-32,255,000 , GRCh37.p13 chr21: 33,618,113-33,627,312 MIS18A
    nsv7032526copy number variation1nstd229human GRCh38 chr21: 32,146,301-32,157,000 , GRCh37.p13 chr21: 33,518,612-33,529,312 MIS18A
    nsv7032521copy number variation1nstd229human GRCh38 chr21: 32,203,395-32,210,458 , GRCh37.p13 chr21: 33,575,707-33,582,770 MIS18A
    nsv7032354copy number variation1nstd229human GRCh38 chr21: 32,180,029-32,186,123 , GRCh37.p13 chr21: 33,552,341-33,558,435 MIS18A
    nsv7031354copy number variation1nstd229human GRCh38 chr21: 32,193,120-32,198,030 , GRCh37.p13 chr21: 33,565,432-33,570,342 MIS18A
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