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Items: 1 to 20 of 313

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672810copy number variation1nstd102humanPathogenic GRCh38 chr14: 73,204,758-73,209,313 , GRCh37 chr14: 73,671,466-73,676,021 PSEN1
    nsv6309359copy number variation1nstd102humanPathogenic GRCh37 chr14: 73,673,074-73,673,200 , GRCh38.p12 chr14: 73,206,366-73,206,492 PSEN1
    nsv3878794copy number variation1nstd102humannot provided GRCh37 chr14: 73,671,094-73,676,951 , GRCh38 chr14: 73,204,386-73,210,243 PSEN1
    nsv5672571copy number variation1nstd102humannot provided GRCh37 chr14: 73,671,468-73,676,022 , GRCh38 chr14: 73,204,760-73,209,314 PSEN1
    nsv6490695copy number variation1nstd223human GRCh38 chr14: 73,166,002-73,168,620 , GRCh37.p13 chr14: 73,632,710-73,635,328 PSEN1
    nsv6489559copy number variation1nstd223human GRCh38 chr14: 73,194,801-73,197,100 , GRCh37.p13 chr14: 73,661,509-73,663,808 PSEN1
    nsv6477804copy number variation1nstd223human GRCh38 chr14: 73,200,801-73,202,800 , GRCh37.p13 chr14: 73,667,509-73,669,508 PSEN1
    nsv5500386copy number variation1nstd206human GRCh38 chr14: 73,183,893-73,184,169 , GRCh37.p13 chr14: 73,650,601-73,650,877 PSEN1
    nsv5509672copy number variation1nstd206human GRCh38 chr14: 73,183,420-73,183,524 , GRCh37.p13 chr14: 73,650,128-73,650,232 PSEN1
    nsv6021566copy number variation1nstd212human GRCh38 chr14: 73,201,350-73,202,729 , GRCh37.p13 chr14: 73,668,058-73,669,437 PSEN1
    nsv6026635copy number variation1nstd212human GRCh38 chr14: 73,183,918-73,184,389 , GRCh37.p13 chr14: 73,650,626-73,651,097 PSEN1
    nsv6021505copy number variation1nstd212human GRCh38 chr14: 73,184,384-73,184,515 , GRCh37.p13 chr14: 73,651,092-73,651,223 PSEN1
    nsv6032635copy number variation1nstd212human GRCh38 chr14: 73,138,875-73,138,964 , GRCh37.p13 chr14: 73,605,583-73,605,672 PSEN1
    nsv4737592copy number variation1nstd199human GRCh37 chr14: 73,650,801-73,650,902 , GRCh38.p12 chr14: 73,184,093-73,184,194 PSEN1
    nsv5311958copy number variation1nstd204human GRCh38.p13 chr14: 73,160,676-73,162,389 , GRCh37.p13 chr14: 73,627,384-73,629,097 PSEN1
    nsv5317783copy number variation1nstd204human GRCh38.p13 chr14: 73,201,365-73,202,678 , GRCh37.p13 chr14: 73,668,073-73,669,386 PSEN1
    nsv5309879copy number variation1nstd204human GRCh38.p13 chr14: 73,144,261-73,145,095 , GRCh37.p13 chr14: 73,610,969-73,611,803 PSEN1
    nsv5601607copy number variation1nstd207human GRCh38 chr14: 73,183,893-73,184,168 , GRCh37.p13 chr14: 73,650,601-73,650,876 PSEN1
    nsv5601889copy number variation1nstd207human GRCh38 chr14: 73,184,335-73,184,461 , GRCh37.p13 chr14: 73,651,043-73,651,169 PSEN1
    nsv4999990copy number variation1nstd200human GRCh38 chr14: 73,166,002-73,168,620 , GRCh37.p13 chr14: 73,632,710-73,635,328 PSEN1
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