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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885941copy number variation1nstd209human GRCh38 chr1: 40,392,609-40,392,817 , GRCh37.p13 chr1: 40,858,281-40,858,489 SMAP2
    nsv5878392copy number variation1nstd209human GRCh38 chr1: 40,387,820-40,387,874 , GRCh37.p13 chr1: 40,853,492-40,853,546 SMAP2
    nsv5875311copy number variation1nstd209human GRCh38 chr1: 40,392,039-40,392,384 , GRCh37.p13 chr1: 40,857,711-40,858,056 SMAP2
    nsv5430806copy number variation1nstd206human GRCh38 chr1: 40,375,029-40,406,071 , GRCh37.p13 chr1: 40,840,701-40,871,743 SMAP2
    nsv5428715copy number variation1nstd206human GRCh38 chr1: 40,392,611-40,392,818 , GRCh37.p13 chr1: 40,858,283-40,858,490 SMAP2
    nsv5419166copy number variation1nstd206human GRCh38 chr1: 40,282,326-40,393,224 , GRCh37.p13 chr1: 40,747,998-40,858,896 , COL9A2, 3 more genes
    nsv5414544copy number variation1nstd206human GRCh38 chr1: 40,382,869-40,382,934 , GRCh37.p13 chr1: 40,848,541-40,848,606 SMAP2
    nsv5377581translocation1nstd200human GRCh38 chr1: 40,411,540-40,411,540 , GRCh38 chr1: 4,339,014-4,339,014 , GRCh37.p13 chr1: 4,399,074-4,399,074 , GRCh37.p13 chr1: 40,877,212-40,877,212 SMAP2
    nsv5351287translocation1nstd200human GRCh38 chr1: 40,392,043-40,392,043 , GRCh38 chr1: 40,392,385-40,392,385 , GRCh37.p13 chr1: 40,858,057-40,858,057 , GRCh37.p13 chr1: 40,857,715-40,857,715 SMAP2
    nsv5340275translocation1nstd200human GRCh37 chr1: 40,858,057-40,858,057 , GRCh37 chr1: 40,857,715-40,857,715 , GRCh38.p12 chr1: 40,392,043-40,392,043 , GRCh38.p12 chr1: 40,392,385-40,392,385 SMAP2
    nsv5339235translocation1nstd200human GRCh37 chr1: 40,859,473-40,859,473 , GRCh37 chr1: 40,859,523-40,859,523 , GRCh38.p12 chr1: 40,393,851-40,393,851 , GRCh38.p12 chr1: 40,393,801-40,393,801 SMAP2
    nsv5338923translocation1nstd200human GRCh37 chr1: 40,877,212-40,877,212 , GRCh37 chr1: 4,399,074-4,399,074 , GRCh38.p12 chr1: 4,339,014-4,339,014 , GRCh38.p12 chr1: 40,411,540-40,411,540 SMAP2
    nsv5325843translocation1nstd204human GRCh38.p13 chr1: 40,392,043-40,392,043 , GRCh38.p13 chr1: 40,392,385-40,392,385 , GRCh37.p13 chr1: 40,857,715-40,857,715 , GRCh37.p13 chr1: 40,858,057-40,858,057 SMAP2
    nsv5216922copy number variation1nstd204human GRCh38.p13 chr1: 40,393,359-40,394,458 , GRCh37.p13 chr1: 40,859,031-40,860,130 SMAP2
    nsv5212354copy number variation1nstd204human GRCh38.p13 chr1: 40,368,301-40,409,800 , GRCh37.p13 chr1: 40,833,973-40,875,472 SMAP2
    nsv5066978mobile element insertion1nstd203human GRCh38 chr1: 40,388,807-40,388,821 , GRCh37.p13 chr1: 40,854,479-40,854,493 SMAP2
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4518299copy number variation1nstd166human GRCh37.p13 chr1: 40,813,266-40,873,384 , GRCh38.p12 chr1: 40,347,594-40,407,712 , SMAP2
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