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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888582copy number variation1nstd209human GRCh38 chr3: 46,802,705-48,210,414 , GRCh37.p13 chr3: 46,844,195-48,251,904 SNORD13P3, LOC105377074, 34 more genes
    nsv5836595copy number variation2nstd209human GRCh38 chr3: 47,836,335-47,837,460 , GRCh37.p13 chr3: 47,877,825-47,878,950 DHX30
    nsv5836594copy number variation1nstd209human GRCh38 chr3: 47,836,310-47,842,941 , GRCh37.p13 chr3: 47,877,800-47,884,431 DHX30
    nsv5836593copy number variation1nstd209human GRCh38 chr3: 47,833,008-47,834,307 , GRCh37.p13 chr3: 47,874,498-47,875,797 DHX30
    nsv5836592copy number variation1nstd209human GRCh38 chr3: 47,823,957-47,825,256 , GRCh37.p13 chr3: 47,865,447-47,866,746 DHX30
    nsv5836591copy number variation1nstd209human GRCh38 chr3: 47,800,241-47,804,778 , GRCh37.p13 chr3: 47,841,731-47,846,268 DHX30
    nsv5836342copy number variation1nstd209human GRCh38 chr3: 47,815,070-47,821,135 , GRCh37.p13 chr3: 47,856,560-47,862,625 DHX30
    nsv5836039copy number variation1nstd209human GRCh38 chr3: 47,826,857-47,829,010 , GRCh37.p13 chr3: 47,868,347-47,870,500 DHX30
    nsv5689272mobile element insertion1nstd211human GRCh38 chr3: 47,813,864-47,813,864 , GRCh37.p13 chr3: 47,855,354-47,855,354 DHX30
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5451619copy number variation1nstd206human GRCh38 chr3: 47,836,731-47,836,817 , GRCh37.p13 chr3: 47,878,221-47,878,307 DHX30
    nsv5443395copy number variation1nstd206human GRCh38 chr3: 47,821,254-47,823,614 , GRCh37.p13 chr3: 47,862,744-47,865,104 DHX30
    nsv5442745copy number variation1nstd206human GRCh38 chr3: 47,829,709-47,838,243 , GRCh37.p13 chr3: 47,871,199-47,879,733 DHX30
    nsv5202391copy number variation1nstd204human GRCh38.p13 chr3: 47,636,701-47,814,200 , GRCh37.p13 chr3: 47,678,191-47,855,690 DHX30, SMARCC1, 2 more genes
    nsv5077377mobile element insertion1nstd203human GRCh38 chr3: 47,806,031-47,806,031 , GRCh37.p13 chr3: 47,847,521-47,847,521 DHX30
    nsv5066662mobile element insertion1nstd203human GRCh38 chr3: 47,829,314-47,829,330 , GRCh37.p13 chr3: 47,870,804-47,870,820 DHX30
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924397copy number variation1nstd200human GRCh38 chr3: 47,344,940-47,923,420 , GRCh37.p13 chr3: 47,386,430-47,964,910 PTPN23, DHX30, 13 more genes
    nsv4911170copy number variation1nstd200human GRCh38 chr3: 47,835,453-47,839,927 , GRCh37.p13 chr3: 47,876,943-47,881,417 DHX30
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