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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137064copy number variation1nstd102humanLikely pathogenic GRCh38 chr15: 48,508,704-48,534,080 , GRCh37.p13 chr15: 48,800,901-48,826,277 FBN1
    nsv7094717copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,826,257-49,097,846 , GRCh38.p12 chr15: 48,534,060-48,805,649 FBN1, CEP152, 2 more genes
    nsv7094716copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,773,832-48,936,966 , GRCh38.p12 chr15: 48,481,635-48,644,769 FBN1-DT, FBN1
    nsv7094715copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,733,898-48,734,063 , GRCh38.p12 chr15: 48,441,701-48,441,866 FBN1
    nsv7094714copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,729,138-48,748,979 , GRCh38.p12 chr15: 48,436,941-48,456,782 FBN1
    nsv7094713copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,720,523-48,725,205 , GRCh38.p12 chr15: 48,428,326-48,433,008 FBN1
    nsv7094544copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,805,726-48,808,579 , GRCh38.p12 chr15: 48,513,529-48,516,382 FBN1
    nsv7094543copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,791,162-48,936,966 , GRCh38.p12 chr15: 48,498,965-48,644,769 FBN1-DT, FBN1
    nsv7094542copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,791,162-48,791,255 , GRCh38.p12 chr15: 48,498,965-48,499,058 FBN1
    nsv7094541copy number variation1nstd102humanUncertain significance GRCh37 chr15: 48,729,138-48,730,134 , GRCh38.p12 chr15: 48,436,941-48,437,937 FBN1
    nsv7094540copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,722,912-48,727,571 , GRCh38.p12 chr15: 48,430,715-48,435,374 FBN1
    nsv7094383copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,902,905-48,936,966 , GRCh38.p12 chr15: 48,610,708-48,644,769 FBN1-DT, FBN1
    nsv7094382copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,888,460-48,905,309 , GRCh38.p12 chr15: 48,596,263-48,613,112 FBN1
    nsv7094381copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,888,460-48,888,595 , GRCh38.p12 chr15: 48,596,263-48,596,398 FBN1
    nsv7094380copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,729,138-48,734,063 , GRCh38.p12 chr15: 48,436,941-48,441,866 FBN1
    nsv7094379copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,703,187-48,741,110 , GRCh38.p12 chr15: 48,410,990-48,448,913 FBN1
    nsv7094294copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,703,187-48,713,903 , GRCh38.p12 chr15: 48,410,990-48,421,706 FBN1
    nsv7093607insertion1nstd102humanPathogenic GRCh37 chr15: 48,703,276-48,703,276 , GRCh38 chr15: 48,411,079-48,411,079 FBN1
    nsv7067502inversion1nstd229human GRCh38 chr15: 48,513,881-51,354,383 , GRCh37.p13 chr15: 48,806,078-51,646,580 NDUFAF4P1, MIR4713, 49 more genes
    nsv7065163inversion1nstd229human GRCh38 chr15: 48,595,447-48,595,518 , GRCh37.p13 chr15: 48,887,644-48,887,715 FBN1
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