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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 VAMP8, TMSB10, 86 more genes
    nsv5966038insertion1nstd209human GRCh38 chr2: 85,008,354-85,008,354 , GRCh37.p13 chr2: 85,235,477-85,235,477 KCMF1
    nsv5886172copy number variation1nstd209human GRCh38 chr2: 85,044,550-85,044,692 , GRCh37.p13 chr2: 85,271,673-85,271,815 KCMF1
    nsv5622727insertion1nstd207human GRCh38 chr2: 85,008,354-85,008,354 , GRCh37.p13 chr2: 85,235,477-85,235,477 KCMF1
    nsv5620712insertion1nstd207human GRCh38 chr2: 85,008,312-85,008,312 , GRCh37.p13 chr2: 85,235,435-85,235,435 KCMF1
    nsv5577860copy number variation1nstd207human GRCh38 chr2: 85,008,234-85,008,375 , GRCh37.p13 chr2: 85,235,357-85,235,498 KCMF1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5447085copy number variation1nstd206human GRCh38 chr2: 85,056,935-85,058,142 , GRCh37.p13 chr2: 85,284,058-85,285,265 KCMF1
    nsv5443924copy number variation1nstd206human GRCh38 chr2: 84,979,817-84,981,281 , GRCh37.p13 chr2: 85,206,940-85,208,404 KCMF1
    nsv5443882copy number variation1nstd206human GRCh38 chr2: 85,008,267-85,008,376 , GRCh37.p13 chr2: 85,235,390-85,235,499 KCMF1
    nsv5443441copy number variation1nstd206human GRCh38 chr2: 84,971,083-84,971,147 , GRCh37.p13 chr2: 85,198,206-85,198,270 KCMF1
    nsv5439921copy number variation1nstd206human GRCh38 chr2: 84,981,221-84,982,529 , GRCh37.p13 chr2: 85,208,344-85,209,652 KCMF1
    nsv5434598copy number variation1nstd206human GRCh38 chr2: 84,975,839-84,981,957 , GRCh37.p13 chr2: 85,202,962-85,209,080 KCMF1
    nsv5208709copy number variation1nstd204human GRCh38.p13 chr2: 84,970,515-84,972,902 , GRCh37.p13 chr2: 85,197,638-85,200,025 KCMF1
    nsv5065374mobile element insertion1nstd203human GRCh38 chr2: 85,030,626-85,030,642 , GRCh37.p13 chr2: 85,257,749-85,257,765 KCMF1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908898copy number variation1nstd200human GRCh38 chr2: 84,995,039-84,996,644 , GRCh37.p13 chr2: 85,222,162-85,223,767 KCMF1
    nsv4902347copy number variation1nstd200human GRCh38 chr2: 85,000,267-85,005,422 , GRCh37.p13 chr2: 85,227,390-85,232,545 KCMF1
    nsv4902346copy number variation1nstd200human GRCh38 chr2: 84,996,394-84,997,497 , GRCh37.p13 chr2: 85,223,517-85,224,620 KCMF1
    nsv4902345copy number variation1nstd200human GRCh38 chr2: 84,981,238-84,982,470 , GRCh37.p13 chr2: 85,208,361-85,209,593 KCMF1
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