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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5664778inversion1nstd207human GRCh38 chr1: 152,208,990-152,251,507 , GRCh37.p13 chr1: 152,181,466-152,223,983 HRNR
    nsv5622838insertion1nstd207human GRCh38 chr1: 152,213,624-152,213,624 , GRCh37.p13 chr1: 152,186,100-152,186,100 HRNR
    nsv5622257insertion1nstd207human GRCh38 chr1: 152,215,843-152,215,843 , GRCh37.p13 chr1: 152,188,319-152,188,319 HRNR
    nsv5621204insertion1nstd207human GRCh38 chr1: 152,213,946-152,213,946 , GRCh37.p13 chr1: 152,186,422-152,186,422 HRNR
    nsv5620415insertion2nstd207human GRCh38 chr1: 152,215,736-152,215,736 , GRCh37.p13 chr1: 152,188,212-152,188,212 HRNR
    nsv5617785insertion1nstd207human GRCh38 chr1: 152,218,469-152,218,469 , GRCh37.p13 chr1: 152,190,945-152,190,945 HRNR
    nsv5615182insertion1nstd207human GRCh38 chr1: 152,213,644-152,213,644 , GRCh37.p13 chr1: 152,186,120-152,186,120 HRNR
    nsv5613022insertion2nstd207human GRCh38 chr1: 152,215,469-152,215,469 , GRCh37.p13 chr1: 152,187,945-152,187,945 HRNR
    nsv5612598insertion2nstd207human GRCh38 chr1: 152,213,340-152,213,340 , GRCh37.p13 chr1: 152,185,816-152,185,816 HRNR
    nsv5606025insertion1nstd207human GRCh38 chr1: 152,216,761-152,216,761 , GRCh37.p13 chr1: 152,189,237-152,189,237 HRNR
    nsv5604701insertion1nstd207human GRCh38 chr1: 152,214,597-152,214,597 , GRCh37.p13 chr1: 152,187,073-152,187,073 HRNR
    nsv5572146copy number variation1nstd207human GRCh38 chr1: 152,212,989-152,213,252 , GRCh37.p13 chr1: 152,185,465-152,185,728 HRNR
    nsv5572139copy number variation1nstd207human GRCh38 chr1: 152,213,253-152,214,662 , GRCh37.p13 chr1: 152,185,729-152,187,138 HRNR
    nsv5432184copy number variation1nstd206human GRCh38 chr1: 152,212,587-152,218,300 , GRCh37.p13 chr1: 152,185,063-152,190,776 HRNR
    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
    nsv5219673copy number variation1nstd204human GRCh38.p13 chr1: 152,213,801-152,215,300 , GRCh37.p13 chr1: 152,186,277-152,187,776 HRNR
    nsv5216942copy number variation1nstd204human GRCh38.p13 chr1: 152,215,501-152,217,000 , GRCh37.p13 chr1: 152,187,977-152,189,476 HRNR
    nsv5212431copy number variation1nstd204human GRCh38.p13 chr1: 152,213,401-152,218,000 , GRCh37.p13 chr1: 152,185,877-152,190,476 HRNR
    nsv5210611copy number variation1nstd204human GRCh38.p13 chr1: 152,215,401-152,220,300 , GRCh37.p13 chr1: 152,187,877-152,192,776 HRNR
    nsv5203565copy number variation1nstd204human GRCh38.p13 chr1: 152,213,601-152,223,200 , GRCh37.p13 chr1: 152,186,077-152,195,676 HRNR
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