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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4451832copy number variation1nstd102humanPathogenic GRCh38 chr9: 132,896,215-132,928,892 , GRCh37 chr9: 135,771,602-135,804,279 TSC1
    nsv3872348copy number variation1nstd102humanPathogenic GRCh38 chr9: 132,896,229-132,928,878 , GRCh37 chr9: 135,771,616-135,804,265 TSC1
    nsv4682244copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,775,735-135,797,380 , GRCh38.p12 chr9: 132,900,348-132,921,993 TSC1
    nsv4683975copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,785,938-135,804,279 , GRCh38.p12 chr9: 132,910,551-132,928,892 TSC1
    nsv5673820copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,782,098-135,796,843 , GRCh38.p12 chr9: 132,906,711-132,921,456 TSC1
    nsv7097934copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,771,184-135,781,738 , GRCh38.p12 chr9: 132,895,797-132,906,351 TSC1
    nsv3878833copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,771,602-135,779,861 , GRCh38 chr9: 132,896,215-132,904,474 TSC1
    nsv5564453copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,777,972-135,782,777 , GRCh38.p12 chr9: 132,902,585-132,907,390 TSC1
    nsv4681771copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,771,602-135,776,244 , GRCh38.p12 chr9: 132,896,215-132,900,857 TSC1
    nsv4728171copy number variation1nstd102humanPathogenic GRCh38 chr9: 132,902,018-132,904,171 , GRCh37 chr9: 135,777,405-135,779,558 TSC1
    nsv3873528copy number variation1nstd102humanPathogenic GRCh38 chr9: 132,910,551-132,912,477 , GRCh37 chr9: 135,785,938-135,787,864 TSC1
    nsv6313261copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,802,568-135,804,339 , GRCh38.p12 chr9: 132,927,181-132,928,952 TSC1
    nsv4728593copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,776,875-135,778,432 , GRCh38 chr9: 132,901,488-132,903,045 TSC1
    nsv7098430copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,771,622-135,773,017 , GRCh38.p12 chr9: 132,896,235-132,897,630 TSC1
    nsv4681344copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,796,730-135,797,380 , GRCh38.p12 chr9: 132,921,343-132,921,993 TSC1
    nsv4683739copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,772,551-135,773,017 , GRCh38.p12 chr9: 132,897,164-132,897,630 TSC1
    nsv7098067copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,798,715-135,798,899 , GRCh38.p12 chr9: 132,923,328-132,923,512 TSC1
    nsv4681169copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,802,568-135,802,711 , GRCh38.p12 chr9: 132,927,181-132,927,324 TSC1
    nsv3887613copy number variation1nstd102humanPathogenic GRCh37 chr9: 135,776,102-135,787,844 , GRCh38 chr9: 132,900,715-132,912,457 TSC1
    nsv4684000insertion1nstd102humanPathogenic GRCh37 chr9: 135,800,976-135,800,976 , GRCh38 chr9: 132,925,589-132,925,589 TSC1
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