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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120738copy number variation1nstd186human GRCh37 chr14: 76,091,261-76,091,393 , GRCh38.p12 chr14: 75,624,918-75,625,050 FLVCR2
    nsv5977610insertion1nstd209human GRCh38 chr14: 75,594,206-75,594,206 , GRCh37.p13 chr14: 76,060,549-76,060,549 FLVCR2, RPS24P2
    nsv5975586inversion1nstd209human GRCh38 chr14: 75,625,183-75,626,225 , GRCh37.p13 chr14: 76,091,526-76,092,568 FLVCR2
    nsv5945910copy number variation1nstd209human GRCh38 chr14: 75,591,457-75,591,507 , GRCh37.p13 chr14: 76,057,800-76,057,850 FLVCR2
    nsv5939055copy number variation1nstd209human GRCh38 chr14: 75,596,184-75,596,235 , GRCh37.p13 chr14: 76,062,527-76,062,578 RPS24P2, FLVCR2
    nsv5855730copy number variation1nstd209human GRCh38 chr14: 75,625,165-75,627,364 , GRCh37.p13 chr14: 76,091,508-76,093,707 FLVCR2
    nsv5707764mobile element insertion1nstd211human GRCh38 chr14: 75,607,383-75,607,383 , GRCh37.p13 chr14: 76,073,726-76,073,726 RNA5SP387, FLVCR2
    nsv5697847mobile element insertion2nstd211human GRCh38 chr14: 75,594,222-75,594,222 , GRCh37.p13 chr14: 76,060,565-76,060,565 FLVCR2, RPS24P2
    nsv5695862mobile element insertion2nstd211human GRCh38 chr14: 75,587,479-75,587,479 , GRCh37.p13 chr14: 76,053,822-76,053,822 FLVCR2
    nsv5648683insertion1nstd207human GRCh38 chr14: 75,625,200-75,625,200 , GRCh37.p13 chr14: 76,091,543-76,091,543 FLVCR2
    nsv5646350insertion1nstd207human GRCh38 chr14: 75,629,499-75,629,499 , GRCh37.p13 chr14: 76,095,842-76,095,842 FLVCR2
    nsv5603691copy number variation1nstd207human GRCh38 chr14: 75,624,917-75,625,098 , GRCh37.p13 chr14: 76,091,260-76,091,441 FLVCR2
    nsv5594134copy number variation1nstd207human GRCh38 chr14: 75,625,236-75,627,372 , GRCh37.p13 chr14: 76,091,579-76,093,715 FLVCR2
    nsv5557478sequence alteration1nstd206human GRCh38 chr14: 75,625,186-75,627,373 , GRCh37.p13 chr14: 76,091,529-76,093,716 FLVCR2
    nsv5539077insertion1nstd206human GRCh38 chr14: 75,607,383-75,607,419 , GRCh37.p13 chr14: 76,073,726-76,073,762 FLVCR2, RNA5SP387
    nsv5498240copy number variation1nstd206human GRCh38 chr14: 75,624,918-75,625,050 , GRCh37.p13 chr14: 76,091,261-76,091,393 FLVCR2
    nsv5432412mobile element insertion1nstd206human GRCh38 chr14: 75,587,479-75,587,530 , GRCh37.p13 chr14: 76,053,822-76,053,873 FLVCR2
    nsv5416506mobile element insertion1nstd206human GRCh38 chr14: 75,594,222-75,594,273 , GRCh37.p13 chr14: 76,060,565-76,060,616 RPS24P2, FLVCR2
    nsv5391734copy number variation1nstd186human GRCh37 chr14: 76,091,260-76,093,716 , GRCh38.p12 chr14: 75,624,917-75,627,373 FLVCR2
    nsv5374611translocation1nstd200human GRCh38 chr14: 75,627,374-75,627,374 , GRCh38 chr14: 75,626,074-75,626,074 , GRCh37.p13 chr14: 76,093,717-76,093,717 , GRCh37.p13 chr14: 76,092,417-76,092,417 FLVCR2
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