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Items: 1 to 20 of 566

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958178insertion1nstd209human GRCh38 chr9: 32,936,349-32,936,349 , GRCh37.p13 chr9: 32,936,347-32,936,347 APTX
    nsv5951484insertion1nstd209human GRCh38 chr9: 32,883,288-32,883,288 , GRCh37.p13 chr9: 32,883,286-32,883,286 APTX
    nsv5922857copy number variation1nstd209human GRCh38 chr9: 33,014,588-33,014,662 , GRCh37.p13 chr9: 33,014,586-33,014,660 APTX
    nsv5919097copy number variation1nstd209human GRCh38 chr9: 32,900,626-32,901,115 , GRCh37.p13 chr9: 32,900,624-32,901,113 APTX
    nsv5915819copy number variation1nstd209human GRCh38 chr9: 32,916,356-32,916,426 , GRCh37.p13 chr9: 32,916,354-32,916,424 APTX
    nsv5913717copy number variation1nstd209human GRCh38 chr9: 32,892,296-32,892,397 , GRCh37.p13 chr9: 32,892,294-32,892,395 APTX
    nsv5913273copy number variation1nstd209human GRCh38 chr9: 32,906,966-32,907,043 , GRCh37.p13 chr9: 32,906,964-32,907,041 APTX
    nsv5860867copy number variation1nstd209human GRCh38 chr9: 32,952,679-32,954,678 , GRCh37.p13 chr9: 32,952,677-32,954,676 APTX
    nsv5706259mobile element insertion1nstd211human GRCh38 chr9: 32,899,582-32,899,582 , GRCh37.p13 chr9: 32,899,580-32,899,580 APTX
    nsv5705293mobile element insertion2nstd211human GRCh38 chr9: 32,936,365-32,936,365 , GRCh37.p13 chr9: 32,936,363-32,936,363 APTX
    nsv5700858mobile element insertion1nstd211human GRCh38 chr9: 32,938,462-32,938,462 , GRCh37.p13 chr9: 32,938,460-32,938,460 APTX
    nsv5697564mobile element insertion1nstd211human GRCh38 chr9: 32,893,503-32,893,503 , GRCh37.p13 chr9: 32,893,501-32,893,501 APTX
    nsv5643649insertion1nstd207human GRCh38 chr9: 32,906,886-32,906,886 , GRCh37.p13 chr9: 32,906,884-32,906,884 APTX
    nsv5635340insertion1nstd207human GRCh38 chr9: 32,936,349-32,936,349 , GRCh37.p13 chr9: 32,936,347-32,936,347 APTX
    nsv5629833insertion1nstd207human GRCh38 chr9: 32,892,296-32,892,296 , GRCh37.p13 chr9: 32,892,294-32,892,294 APTX
    nsv5628689insertion1nstd207human GRCh38 chr9: 32,892,381-32,892,381 , GRCh37.p13 chr9: 32,892,379-32,892,379 APTX
    nsv5627371insertion1nstd207human GRCh38 chr9: 32,892,294-32,892,294 , GRCh37.p13 chr9: 32,892,292-32,892,292 APTX
    nsv5627103insertion2nstd207human GRCh38 chr9: 32,900,611-32,900,611 , GRCh37.p13 chr9: 32,900,609-32,900,609 APTX
    nsv5627053insertion1nstd207human GRCh38 chr9: 32,883,291-32,883,291 , GRCh37.p13 chr9: 32,883,289-32,883,289 APTX
    nsv5588669copy number variation1nstd207human GRCh38 chr9: 32,900,616-32,900,860 , GRCh37.p13 chr9: 32,900,614-32,900,858 APTX
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