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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976708inversion1nstd209human GRCh38 chr1: 29,552,233-30,655,831 , GRCh37.p13 chr1: 30,028,083-31,128,678 LINC01648, LOC105378617, 2 more genes
    nsv5950482insertion1nstd209human GRCh38 chr1: 30,036,651-30,036,651 , GRCh37.p13 chr1: 30,509,498-30,509,498 LINC01648
    nsv5885891copy number variation1nstd209human GRCh38 chr1: 30,006,936-30,016,624 , GRCh37.p13 chr1: 30,479,783-30,489,471 LINC01648
    nsv5869754copy number variation1nstd209human GRCh38 chr1: 30,034,213-30,035,492 , GRCh37.p13 chr1: 30,507,060-30,508,339 LINC01648
    nsv5829982copy number variation1nstd209human GRCh38 chr1: 30,006,801-30,016,595 , GRCh37.p13 chr1: 30,479,648-30,489,442 LINC01648
    nsv5829950copy number variation1nstd209human GRCh38 chr1: 30,034,221-30,035,520 , GRCh37.p13 chr1: 30,507,068-30,508,367 LINC01648
    nsv5429369copy number variation1nstd206human GRCh38 chr1: 30,033,952-30,035,493 , GRCh37.p13 chr1: 30,506,799-30,508,340 LINC01648
    nsv5425856copy number variation1nstd206human GRCh38 chr1: 29,769,382-30,451,469 , GRCh37.p13 chr1: 30,242,229-30,924,316 LINC01648, LOC105378617, 1 more genes
    nsv5417299copy number variation1nstd206human GRCh38 chr1: 30,006,936-30,016,625 , GRCh37.p13 chr1: 30,479,783-30,489,472 LINC01648
    nsv5380576translocation1nstd200human GRCh38 chr1: 30,035,489-30,035,489 , GRCh38 chr1: 30,034,212-30,034,212 , GRCh37.p13 chr1: 30,508,336-30,508,336 , GRCh37.p13 chr1: 30,507,059-30,507,059 LINC01648
    nsv5296183copy number variation1nstd204human GRCh38.p13 chr1: 30,006,930-30,016,628 , GRCh37.p13 chr1: 30,479,777-30,489,475 LINC01648
    nsv5291462copy number variation1nstd204human GRCh38.p13 chr1: 30,034,182-30,035,517 , GRCh37.p13 chr1: 30,507,029-30,508,364 LINC01648
    nsv5215390copy number variation1nstd204human GRCh38.p13 chr1: 30,006,901-30,016,645 , GRCh37.p13 chr1: 30,479,748-30,489,492 LINC01648
    nsv5213882copy number variation1nstd204human GRCh38.p13 chr1: 30,034,221-30,035,720 , GRCh37.p13 chr1: 30,507,068-30,508,567 LINC01648
    nsv5210958copy number variation1nstd204human GRCh38.p13 chr1: 30,006,901-30,016,600 , GRCh37.p13 chr1: 30,479,748-30,489,447 LINC01648
    nsv4895700copy number variation1nstd200human GRCh38 chr1: 30,006,936-30,016,625 , GRCh37.p13 chr1: 30,479,783-30,489,472 LINC01648
    nsv4772883copy number variation1nstd200human GRCh37 chr1: 30,507,037-30,508,350 , GRCh38.p12 chr1: 30,034,190-30,035,503 LINC01648
    nsv4772882copy number variation1nstd200human GRCh37 chr1: 30,479,783-30,489,472 , GRCh38.p12 chr1: 30,006,936-30,016,625 LINC01648
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4767570inversion1nstd199human GRCh38.p12 chr1: 29,551,565-30,656,490 , GRCh37 chr1: 29,878,077-31,129,337 LINC01648, LOC105378617, 2 more genes
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