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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116949mobile element insertion1nstd186human GRCh37 chr1: 177,924,283-177,924,334 , GRCh38.p12 chr1: 177,955,148-177,955,199 SEC16B, CRYZL2P-SEC16B
    nsv5887368copy number variation1nstd209human GRCh38 chr1: 177,936,028-177,936,938 , GRCh37.p13 chr1: 177,905,163-177,906,073 SEC16B, CRYZL2P-SEC16B
    nsv5877594copy number variation1nstd209human GRCh38 chr1: 177,962,907-177,963,402 , GRCh37.p13 chr1: 177,932,042-177,932,537 SEC16B, CRYZL2P-SEC16B
    nsv5870850copy number variation1nstd209human GRCh38 chr1: 177,978,760-177,985,161 , GRCh37.p13 chr1: 177,947,895-177,954,296 CRYZL2P-SEC16B, SEC16B
    nsv5685548mobile element insertion2nstd211human GRCh38 chr1: 177,955,148-177,955,148 , GRCh37.p13 chr1: 177,924,283-177,924,283 SEC16B, CRYZL2P-SEC16B
    nsv5676023mobile element insertion1nstd211human GRCh38 chr1: 177,968,696-177,968,696 , GRCh37.p13 chr1: 177,937,831-177,937,831 SEC16B, CRYZL2P-SEC16B
    nsv5675502mobile element insertion2nstd211human GRCh38 chr1: 177,957,338-177,957,338 , GRCh37.p13 chr1: 177,926,473-177,926,473 SEC16B, CRYZL2P-SEC16B
    nsv5423587copy number variation1nstd206human GRCh38 chr1: 177,977,110-177,982,798 , GRCh37.p13 chr1: 177,946,245-177,951,933 CRYZL2P-SEC16B, SEC16B
    nsv5422410copy number variation1nstd206human GRCh38 chr1: 177,962,896-177,963,403 , GRCh37.p13 chr1: 177,932,031-177,932,538 CRYZL2P-SEC16B, SEC16B
    nsv5421295copy number variation1nstd206human GRCh38 chr1: 177,982,661-177,988,170 , GRCh37.p13 chr1: 177,951,796-177,957,305 CRYZL2P-SEC16B, SEC16B
    nsv5406012mobile element insertion1nstd206human GRCh38 chr1: 177,968,696-177,968,747 , GRCh37.p13 chr1: 177,937,831-177,937,882 CRYZL2P-SEC16B, SEC16B
    nsv5400144mobile element insertion1nstd206human GRCh38 chr1: 177,957,338-177,957,389 , GRCh37.p13 chr1: 177,926,473-177,926,524 CRYZL2P-SEC16B, SEC16B
    nsv5394391mobile element insertion1nstd206human GRCh38 chr1: 177,955,148-177,955,199 , GRCh37.p13 chr1: 177,924,283-177,924,334 CRYZL2P-SEC16B, SEC16B
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5347332translocation1nstd200human GRCh38 chr1: 177,977,110-177,977,110 , GRCh38 chr1: 177,982,798-177,982,798 , GRCh37.p13 chr1: 177,946,245-177,946,245 , GRCh37.p13 chr1: 177,951,933-177,951,933 SEC16B, CRYZL2P-SEC16B
    nsv5288003copy number variation1nstd204human GRCh37.p13 chr1: 177,784,611-178,417,549 , GRCh38.p13 chr1: 177,815,476-178,448,414 RASAL2, SEC16B, 6 more genes
    nsv5219635copy number variation1nstd204human GRCh37.p13 chr1: 177,784,636-178,131,135 , GRCh38.p13 chr1: 177,815,501-178,162,000 RASAL2, SEC16B, 4 more genes
    nsv5076191mobile element insertion1nstd203human GRCh38 chr1: 177,957,322-177,957,338 , GRCh37.p13 chr1: 177,926,457-177,926,473 SEC16B, CRYZL2P-SEC16B
    nsv5071427mobile element insertion1nstd203human GRCh38 chr1: 177,955,137-177,955,148 , GRCh37.p13 chr1: 177,924,272-177,924,283 CRYZL2P-SEC16B, SEC16B
    nsv4904051copy number variation1nstd200human GRCh38 chr1: 177,700,403-177,942,214 , GRCh37.p13 chr1: 177,669,538-177,911,349 LINC01741, SEC16B, 1 more genes
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