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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122111copy number variation1nstd186human GRCh37 chr12: 122,377,453-122,377,525 , GRCh38.p12 chr12: 121,939,547-121,939,619 CFAP251
    nsv5976094insertion1nstd209human GRCh38 chr12: 121,978,393-121,978,393 , GRCh37.p13 chr12: 122,416,299-122,416,299 CFAP251
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5945235copy number variation1nstd209human GRCh38 chr12: 121,939,547-121,939,618 , GRCh37.p13 chr12: 122,377,453-122,377,524 CFAP251
    nsv5939551copy number variation1nstd209human GRCh38 chr12: 121,976,886-121,977,936 , GRCh37.p13 chr12: 122,414,792-122,415,842 CFAP251
    nsv5935981copy number variation1nstd209human GRCh38 chr12: 121,958,626-121,958,705 , GRCh37.p13 chr12: 122,396,532-122,396,611 CFAP251
    nsv5934233copy number variation1nstd209human GRCh38 chr12: 121,945,492-121,945,948 , GRCh37.p13 chr12: 122,383,398-122,383,854 CFAP251
    nsv5857890copy number variation1nstd209human GRCh38 chr12: 121,946,202-121,948,101 , GRCh37.p13 chr12: 122,384,108-122,386,007 CFAP251
    nsv5852487copy number variation1nstd209human GRCh38 chr12: 121,966,687-121,968,834 , GRCh37.p13 chr12: 122,404,593-122,406,740 CFAP251
    nsv5602132copy number variation1nstd207human GRCh38 chr12: 121,939,547-121,939,618 , GRCh37.p13 chr12: 122,377,453-122,377,524 CFAP251
    nsv5601613copy number variation1nstd207human GRCh38 chr12: 121,993,812-121,994,119 , GRCh37.p13 chr12: 122,431,718-122,432,025 CFAP251
    nsv5592824copy number variation1nstd207human GRCh38 chr12: 121,958,626-121,958,705 , GRCh37.p13 chr12: 122,396,532-122,396,611 CFAP251
    nsv5585656copy number variation1nstd207human GRCh38 chr12: 121,993,972-121,994,021 , GRCh37.p13 chr12: 122,431,878-122,431,927 CFAP251
    nsv5556000sequence alteration1nstd206human GRCh38 chr12: 121,979,753-121,981,247 , GRCh37.p13 chr12: 122,417,659-122,419,153 CFAP251
    nsv5513355copy number variation1nstd206human GRCh38 chr12: 121,971,884-121,972,213 , GRCh37.p13 chr12: 122,409,790-122,410,119 CFAP251
    nsv5509820copy number variation1nstd206human GRCh38 chr12: 121,979,682-121,993,232 , GRCh37.p13 chr12: 122,417,588-122,431,138 CFAP251
    nsv5507964copy number variation1nstd206human GRCh38 chr12: 121,939,547-121,939,619 , GRCh37.p13 chr12: 122,377,453-122,377,525 CFAP251
    nsv5506103copy number variation1nstd206human GRCh38 chr12: 121,979,802-121,981,279 , GRCh37.p13 chr12: 122,417,708-122,419,185 CFAP251
    nsv5505968copy number variation1nstd206human GRCh38 chr12: 121,977,836-121,978,271 , GRCh37.p13 chr12: 122,415,742-122,416,177 CFAP251
    nsv5500819copy number variation1nstd206human GRCh38 chr12: 121,918,070-121,918,169 , GRCh37.p13 chr12: 122,355,976-122,356,075 PSMD9, CFAP251
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