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Items: 1 to 20 of 445

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923552copy number variation1nstd209human GRCh38 chr9: 79,832,552-79,838,805 , GRCh37.p13 chr9: 82,447,467-82,453,720 LOC105376334, LINC01507
    nsv5922952copy number variation1nstd209human GRCh38 chr9: 79,865,752-79,866,129 , GRCh37.p13 chr9: 82,480,667-82,481,044 NPAP1P6, LINC01507, 1 more genes
    nsv5917854copy number variation1nstd209human GRCh38 chr9: 79,846,370-79,846,476 , GRCh37.p13 chr9: 82,461,285-82,461,391 LINC01507, LOC105376334
    nsv5911491copy number variation1nstd209human GRCh38 chr9: 79,860,573-79,860,916 , GRCh37.p13 chr9: 82,475,488-82,475,831 LINC01507, LOC105376101
    nsv5858999copy number variation1nstd209human GRCh38 chr9: 79,832,683-79,838,757 , GRCh37.p13 chr9: 82,447,598-82,453,672 LOC105376334, LINC01507
    nsv5725590mobile element insertion1nstd211human GRCh38 chr9: 79,848,638-79,848,638 , GRCh37.p13 chr9: 82,463,553-82,463,553 LOC105376334, LINC01507
    nsv5715354mobile element insertion1nstd211human GRCh38 chr9: 79,848,621-79,848,621 , GRCh37.p13 chr9: 82,463,536-82,463,536 LINC01507, LOC105376334
    nsv5713137mobile element insertion1nstd211human GRCh38 chr9: 79,967,532-79,967,532 , GRCh37.p13 chr9: 82,582,447-82,582,447 LINC01507
    nsv5704588mobile element insertion2nstd211human GRCh38 chr9: 79,880,208-79,880,208 , GRCh37.p13 chr9: 82,495,123-82,495,123 LINC01507, LOC105376101
    nsv5641755insertion1nstd207human GRCh38 chr9: 79,848,621-79,848,621 , GRCh37.p13 chr9: 82,463,536-82,463,536 LOC105376334, LINC01507
    nsv5634368insertion1nstd207human GRCh38 chr9: 79,934,229-79,934,229 , GRCh37.p13 chr9: 82,549,144-82,549,144 LINC01507
    nsv5625917insertion1nstd207human GRCh38 chr9: 79,987,039-79,987,039 , GRCh37.p13 chr9: 82,601,954-82,601,954 LINC01507, LOC105376099
    nsv5603554copy number variation1nstd207human GRCh38 chr9: 79,987,000-79,987,057 , GRCh37.p13 chr9: 82,601,915-82,601,972 LINC01507, LOC105376099
    nsv5564083mobile element insertion1nstd206human GRCh38 chr9: 79,848,638-79,848,672 , GRCh37.p13 chr9: 82,463,553-82,463,587 LINC01507, LOC105376334
    nsv5545848insertion1nstd206human GRCh38 chr9: 79,825,840-79,825,885 , GRCh37.p13 chr9: 82,440,755-82,440,800 LOC105376334, LINC01507
    nsv5492330copy number variation1nstd206human GRCh38 chr9: 79,860,575-79,860,917 , GRCh37.p13 chr9: 82,475,490-82,475,832 LOC105376101, LINC01507
    nsv5488082copy number variation1nstd206human GRCh38 chr9: 79,961,688-79,961,831 , GRCh37.p13 chr9: 82,576,603-82,576,746 LINC01507
    nsv5488065copy number variation1nstd206human GRCh38 chr9: 79,832,553-79,838,806 , GRCh37.p13 chr9: 82,447,468-82,453,721 LINC01507, LOC105376334
    nsv5487597copy number variation1nstd206human GRCh38 chr9: 79,999,682-80,006,454 , GRCh37.p13 chr9: 82,614,597-82,621,369 LINC01507
    nsv5484369copy number variation1nstd206human GRCh38 chr9: 79,993,393-80,002,383 , GRCh37.p13 chr9: 82,608,308-82,617,298 LINC01507
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