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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941998copy number variation1nstd209human GRCh38 chr15: 42,551,897-42,552,833 , GRCh37.p13 chr15: 42,844,095-42,845,031 HAUS2
    nsv5648374insertion1nstd207human GRCh38 chr15: 42,557,411-42,557,411 , GRCh37.p13 chr15: 42,849,609-42,849,609 HAUS2
    nsv5505727copy number variation1nstd206human GRCh38 chr15: 42,553,136-42,554,808 , GRCh37.p13 chr15: 42,845,334-42,847,006 HAUS2
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5380045translocation1nstd200human GRCh38 chr15: 42,547,260-42,547,260 , GRCh38 chr15: 42,544,125-42,544,125 , GRCh37.p13 chr15: 42,836,323-42,836,323 , GRCh37.p13 chr15: 42,839,458-42,839,458 LRRC57, HAUS2
    nsv5370477translocation1nstd200human GRCh38 chr15: 42,548,744-42,548,744 , GRCh38 chr7: 30,399,999-30,399,999 , GRCh37.p13 chr15: 42,840,942-42,840,942 , GRCh37.p13 chr7: 30,439,615-30,439,615 HAUS2, LRRC57, 1 more genes
    nsv5357860translocation1nstd200human GRCh38 chr15: 42,547,529-42,547,529 , GRCh38 chr15: 42,548,105-42,548,105 , GRCh37.p13 chr15: 42,840,303-42,840,303 , GRCh37.p13 chr15: 42,839,727-42,839,727 LRRC57, HAUS2
    nsv5357859translocation1nstd200human GRCh38 chr15: 42,545,264-42,545,264 , GRCh38 chr15: 42,547,260-42,547,260 , GRCh37.p13 chr15: 42,837,462-42,837,462 , GRCh37.p13 chr15: 42,839,458-42,839,458 LRRC57, HAUS2
    nsv5345212translocation1nstd200human GRCh37 chr15: 42,839,458-42,839,458 , GRCh37 chr15: 42,836,323-42,836,323 , GRCh38.p12 chr15: 42,547,260-42,547,260 , GRCh38.p12 chr15: 42,544,125-42,544,125 HAUS2, LRRC57
    nsv5342357translocation1nstd200human GRCh37 chr7: 30,439,615-30,439,615 , GRCh37 chr15: 42,840,942-42,840,942 , GRCh38.p12 chr15: 42,548,744-42,548,744 , GRCh38.p12 chr7: 30,399,999-30,399,999 HAUS2, LRRC57, 1 more genes
    nsv5337499translocation1nstd200human GRCh37 chr15: 42,840,303-42,840,303 , GRCh37 chr15: 42,839,727-42,839,727 , GRCh38.p12 chr15: 42,547,529-42,547,529 , GRCh38.p12 chr15: 42,548,105-42,548,105 HAUS2, LRRC57
    nsv5335731translocation1nstd200human GRCh37 chr15: 42,839,458-42,839,458 , GRCh37 chr15: 42,837,462-42,837,462 , GRCh38.p12 chr15: 42,545,264-42,545,264 , GRCh38.p12 chr15: 42,547,260-42,547,260 LRRC57, HAUS2
    nsv5143183mobile element insertion1nstd203human GRCh38 chr15: 42,550,284-42,550,321 , GRCh37.p13 chr15: 42,842,482-42,842,519 HAUS2
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5001483copy number variation1nstd200human GRCh38 chr15: 42,556,410-42,558,573 , GRCh37.p13 chr15: 42,848,608-42,850,771 HAUS2
    nsv5001482copy number variation1nstd200human GRCh38 chr15: 42,556,256-42,558,578 , GRCh37.p13 chr15: 42,848,454-42,850,776 HAUS2
    nsv5001481copy number variation1nstd200human GRCh38 chr15: 42,556,067-42,558,419 , GRCh37.p13 chr15: 42,848,265-42,850,617 HAUS2
    nsv5001480copy number variation1nstd200human GRCh38 chr15: 42,554,634-42,556,084 , GRCh37.p13 chr15: 42,846,832-42,848,282 HAUS2
    nsv5001479copy number variation1nstd200human GRCh38 chr15: 42,553,263-42,554,737 , GRCh37.p13 chr15: 42,845,461-42,846,935 HAUS2
    nsv5001478copy number variation1nstd200human GRCh38 chr15: 42,550,721-42,558,599 , GRCh37.p13 chr15: 42,842,919-42,850,797 HAUS2
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