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Items: 1 to 20 of 290

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966989insertion1nstd209human GRCh38 chr9: 128,865,326-128,865,326 , GRCh37.p13 chr9: 131,627,605-131,627,605 KYAT1
    nsv5910703copy number variation1nstd209human GRCh38 chr9: 128,858,145-128,858,445 , GRCh37.p13 chr9: 131,620,424-131,620,724 KYAT1
    nsv5859928copy number variation1nstd209human GRCh38 chr9: 128,839,640-128,844,925 , GRCh37.p13 chr9: 131,601,919-131,607,204 KYAT1
    nsv5856918copy number variation1nstd209human GRCh38 chr9: 128,854,403-128,856,527 , GRCh37.p13 chr9: 131,616,682-131,618,806 KYAT1
    nsv5492195copy number variation1nstd206human GRCh38 chr9: 128,841,100-128,846,198 , GRCh37.p13 chr9: 131,603,379-131,608,477 KYAT1
    nsv5313788copy number variation1nstd204human GRCh38.p13 chr9: 128,841,296-128,842,913 , GRCh37.p13 chr9: 131,603,575-131,605,192 KYAT1
    nsv5304347copy number variation1nstd204human GRCh38.p13 chr9: 128,874,196-128,875,480 , GRCh37.p13 chr9: 131,636,475-131,637,759 KYAT1
    nsv5241889copy number variation1nstd204human GRCh38.p13 chr9: 128,441,101-129,240,100 , GRCh37.p13 chr9: 131,203,380-132,002,379 , KYAT1, 32 more genes
    nsv5241007copy number variation1nstd204human GRCh38.p13 chr9: 128,841,301-128,843,000 , GRCh37.p13 chr9: 131,603,580-131,605,279 KYAT1
    nsv5138963mobile element insertion1nstd203human GRCh38 chr9: 128,872,605-128,872,638 , GRCh37.p13 chr9: 131,634,884-131,634,917 KYAT1
    nsv5138363mobile element insertion1nstd203human GRCh38 chr9: 128,849,616-128,849,629 , GRCh37.p13 chr9: 131,611,895-131,611,908 KYAT1
    nsv5133359mobile element insertion1nstd203human GRCh38 chr9: 128,849,619-128,849,629 , GRCh37.p13 chr9: 131,611,898-131,611,908 KYAT1
    nsv5133140mobile element insertion1nstd203human GRCh38 chr9: 128,852,875-128,852,891 , GRCh37.p13 chr9: 131,615,154-131,615,170 KYAT1
    nsv5124418mobile element insertion1nstd203human GRCh38 chr9: 128,849,620-128,849,629 , GRCh37.p13 chr9: 131,611,899-131,611,908 KYAT1
    nsv5123823mobile element insertion1nstd203human GRCh38 chr9: 128,849,617-128,849,629 , GRCh37.p13 chr9: 131,611,896-131,611,908 KYAT1
    nsv4988420copy number variation1nstd200human GRCh38 chr9: 128,864,906-128,869,091 , GRCh37.p13 chr9: 131,627,185-131,631,370 KYAT1
    nsv4988419copy number variation1nstd200human GRCh38 chr9: 128,841,324-128,842,949 , GRCh37.p13 chr9: 131,603,603-131,605,228 KYAT1
    nsv4988418copy number variation1nstd200human GRCh38 chr9: 128,810,883-128,838,991 , GRCh37.p13 chr9: 131,573,162-131,601,270 ENDOG, TBC1D13, 2 more genes
    nsv4844646copy number variation1nstd200human GRCh37 chr9: 131,603,579-131,605,193 , GRCh38.p12 chr9: 128,841,300-128,842,914 KYAT1
    nsv4769385copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,282,528-131,720,659 , GRCh38.p12 chr9: 128,520,249-128,958,380 LOC101929270, TBC1D13, 20 more genes
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