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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966168insertion1nstd209human GRCh38 chr1: 74,059,339-74,059,339 , GRCh37.p13 chr1: 74,525,023-74,525,023 LRRIQ3
    nsv5869777copy number variation1nstd209human GRCh38 chr1: 74,183,071-74,198,154 , GRCh37.p13 chr1: 74,648,755-74,663,838 FPGT, LRRIQ3, 1 more genes
    nsv5867621copy number variation1nstd209human GRCh38 chr1: 74,051,106-74,051,488 , GRCh37.p13 chr1: 74,516,790-74,517,172 LRRIQ3
    nsv5830749copy number variation3nstd209human GRCh38 chr1: 74,184,269-74,193,569 , GRCh37.p13 chr1: 74,649,953-74,659,253 LRRIQ3
    nsv5830644copy number variation2nstd209human GRCh38 chr1: 74,186,140-74,197,569 , GRCh37.p13 chr1: 74,651,824-74,663,253 FPGT, LRRIQ3, 1 more genes
    nsv5830144copy number variation2nstd209human GRCh38 chr1: 74,181,869-74,188,569 , GRCh37.p13 chr1: 74,647,553-74,654,253 LRRIQ3
    nsv5691047mobile element insertion2nstd211human GRCh38 chr1: 74,059,348-74,059,348 , GRCh37.p13 chr1: 74,525,032-74,525,032 LRRIQ3
    nsv5687801mobile element insertion2nstd211human GRCh38 chr1: 74,163,339-74,163,339 , GRCh37.p13 chr1: 74,629,023-74,629,023 LRRIQ3
    nsv5432514copy number variation1nstd206human GRCh38 chr1: 74,197,460-74,197,706 , GRCh37.p13 chr1: 74,663,144-74,663,390 LRRIQ3, FPGT-TNNI3K, 1 more genes
    nsv5430562copy number variation1nstd206human GRCh38 chr1: 74,162,751-74,162,911 , GRCh37.p13 chr1: 74,628,435-74,628,595 LRRIQ3
    nsv5430535copy number variation1nstd206human GRCh38 chr1: 74,070,685-74,079,246 , GRCh37.p13 chr1: 74,536,369-74,544,930 LRRIQ3
    nsv5427694copy number variation1nstd206human GRCh38 chr1: 74,159,737-74,165,769 , GRCh37.p13 chr1: 74,625,421-74,631,453 LRRIQ3
    nsv5423692copy number variation1nstd206human GRCh38 chr1: 73,622,661-74,248,218 , GRCh37.p13 chr1: 74,088,344-74,713,902 FPGT, TNNI3K, 5 more genes
    nsv5423568copy number variation1nstd206human GRCh38 chr1: 74,078,013-74,078,169 , GRCh37.p13 chr1: 74,543,697-74,543,853 LRRIQ3
    nsv5422996copy number variation1nstd206human GRCh38 chr1: 74,183,071-74,198,157 , GRCh37.p13 chr1: 74,648,755-74,663,841 LRRIQ3, FPGT, 1 more genes
    nsv5414334copy number variation1nstd206human GRCh38 chr1: 74,134,342-74,134,395 , GRCh37.p13 chr1: 74,600,026-74,600,079 LRRIQ3
    nsv5411365mobile element insertion1nstd206human GRCh38 chr1: 74,059,339-74,059,339 , GRCh37.p13 chr1: 74,525,023-74,525,023 LRRIQ3
    nsv5407738mobile element insertion1nstd206human GRCh38 chr1: 74,163,339-74,163,390 , GRCh37.p13 chr1: 74,629,023-74,629,074 LRRIQ3
    nsv5395478mobile element insertion1nstd206human GRCh38 chr1: 74,059,806-74,059,857 , GRCh37.p13 chr1: 74,525,490-74,525,541 LRRIQ3
    nsv5384592copy number variation1nstd186human GRCh37 chr1: 74,648,755-74,663,841 , GRCh38.p12 chr1: 74,183,071-74,198,157 FPGT, LRRIQ3, 1 more genes
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