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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978763inversion1nstd209human GRCh38 chr10: 15,760,449-15,778,094 , GRCh37.p13 chr10: 15,802,448-15,820,093 MINDY3
    nsv5727756mobile element insertion2nstd211human GRCh38 chr10: 15,829,284-15,829,284 , GRCh37.p13 chr10: 15,871,283-15,871,283 MINDY3
    nsv5713611mobile element insertion1nstd211human GRCh38 chr10: 15,832,695-15,832,695 , GRCh37.p13 chr10: 15,874,694-15,874,694 MINDY3
    nsv5710549mobile element insertion2nstd211human GRCh38 chr10: 15,819,021-15,819,021 , GRCh37.p13 chr10: 15,861,020-15,861,020 MINDY3
    nsv5699097mobile element insertion1nstd211human GRCh38 chr10: 15,837,740-15,837,740 , GRCh37.p13 chr10: 15,879,739-15,879,739 MINDY3
    nsv5490093copy number variation1nstd206human GRCh38 chr10: 15,845,099-15,845,192 , GRCh37.p13 chr10: 15,887,098-15,887,191 MINDY3
    nsv5481970copy number variation1nstd206human GRCh38 chr10: 15,839,171-15,839,252 , GRCh37.p13 chr10: 15,881,170-15,881,251 MINDY3
    nsv5476513copy number variation1nstd206human GRCh38 chr10: 15,831,228-15,831,338 , GRCh37.p13 chr10: 15,873,227-15,873,337 MINDY3
    nsv5411047mobile element insertion1nstd206human GRCh38 chr10: 15,837,740-15,837,791 , GRCh37.p13 chr10: 15,879,739-15,879,790 MINDY3
    nsv5402559mobile element insertion1nstd206human GRCh38 chr10: 15,819,021-15,819,072 , GRCh37.p13 chr10: 15,861,020-15,861,071 MINDY3
    nsv5396747mobile element insertion1nstd206human GRCh38 chr10: 15,832,695-15,832,746 , GRCh37.p13 chr10: 15,874,694-15,874,745 MINDY3
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5373238translocation1nstd200human GRCh38 chr10: 15,831,470-15,831,470 , GRCh38 chr10: 15,905,465-15,905,465 , GRCh37.p13 chr10: 15,947,464-15,947,464 , GRCh37.p13 chr10: 15,873,469-15,873,469 MINDY3
    nsv5347542translocation1nstd200human GRCh38 chr10: 15,905,470-15,905,470 , GRCh38 chr10: 15,831,617-15,831,617 , GRCh37.p13 chr10: 15,873,616-15,873,616 , GRCh37.p13 chr10: 15,947,469-15,947,469 MINDY3
    nsv5189107mobile element insertion1nstd203human GRCh38 chr10: 15,829,268-15,829,284 , GRCh37.p13 chr10: 15,871,267-15,871,283 MINDY3
    nsv5180978mobile element insertion1nstd203human GRCh38 chr10: 15,776,538-15,776,551 , GRCh37.p13 chr10: 15,818,537-15,818,550 MINDY3
    nsv5138386mobile element insertion1nstd203human GRCh38 chr10: 15,801,644-15,801,659 , GRCh37.p13 chr10: 15,843,643-15,843,658 MINDY3
    nsv5132445mobile element insertion1nstd203human GRCh38 chr10: 15,776,538-15,776,538 , GRCh37.p13 chr10: 15,818,537-15,818,537 MINDY3
    nsv4975119copy number variation1nstd200human GRCh38 chr10: 15,831,064-15,831,668 , GRCh37.p13 chr10: 15,873,063-15,873,667 MINDY3
    nsv4975118copy number variation1nstd200human GRCh38 chr10: 15,808,921-15,808,996 , GRCh37.p13 chr10: 15,850,920-15,850,995 MINDY3
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