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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148269copy number variation1nstd102humanPathogenic GRCh38 chr8: 37,814,644-38,528,889 , GRCh37.p13 chr8: 37,672,162-38,386,407 GOT1L1, FGFR1, 20 more genes
    nsv7098174copy number variation1nstd102humanPathogenic GRCh37 chr8: 38,314,854-38,314,964 , GRCh38.p12 chr8: 38,457,336-38,457,446 FGFR1
    nsv6312909copy number variation5nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 37,595,441-38,961,219 , GRCh38.p12 chr8: 37,737,923-39,103,700 LSM1, BAG4, 33 more genes
    nsv4681495copy number variation1nstd102humanPathogenic GRCh37 chr8: 38,282,007-38,318,644 , GRCh38.p12 chr8: 38,424,489-38,461,126 FGFR1, RPS20P22
    nsv997149copy number variation1nstd45humanPathogenic GRCh38.p12 chr8: 38,411,138-38,468,834 , GRCh37 chr8: 38,268,656-38,326,352 FGFR1, RPS20P22
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