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Items: 1 to 20 of 449

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958089insertion1nstd209human GRCh38 chr9: 135,892,848-135,892,848 , GRCh37.p13 chr9: 138,784,694-138,784,694 CAMSAP1
    nsv5949575insertion1nstd209human GRCh38 chr9: 135,808,480-135,808,480 , GRCh37.p13 chr9: 138,700,326-138,700,326 CAMSAP1
    nsv5632249insertion1nstd207human GRCh38 chr9: 135,836,690-135,836,690 , GRCh37.p13 chr9: 138,728,536-138,728,536 CAMSAP1
    nsv5630700insertion1nstd207human GRCh38 chr9: 135,847,949-135,847,949 , GRCh37.p13 chr9: 138,739,795-138,739,795 CAMSAP1
    nsv5625867insertion1nstd207human GRCh38 chr9: 135,847,892-135,847,892 , GRCh37.p13 chr9: 138,739,738-138,739,738 CAMSAP1
    nsv5625314insertion1nstd207human GRCh38 chr9: 135,838,227-135,838,227 , GRCh37.p13 chr9: 138,730,073-138,730,073 CAMSAP1
    nsv5488115copy number variation1nstd206human GRCh38 chr9: 135,875,370-135,876,112 , GRCh37.p13 chr9: 138,767,216-138,767,958 CAMSAP1
    nsv5480787copy number variation1nstd206human GRCh38 chr9: 135,887,657-135,887,771 , GRCh37.p13 chr9: 138,779,503-138,779,617 CAMSAP1
    nsv5307165copy number variation1nstd204human GRCh38.p13 chr9: 135,838,074-135,838,748 , GRCh37.p13 chr9: 138,729,920-138,730,594 CAMSAP1
    nsv5037175mobile element deletion1nstd200human GRCh38 chr9: 135,843,781-135,847,197 , GRCh37.p13 chr9: 138,735,627-138,739,043 CAMSAP1
    nsv4985855copy number variation1nstd200human GRCh38 chr9: 135,876,732-135,961,329 , GRCh37.p13 chr9: 138,768,578-138,853,175 CAMSAP1-DT, CAMSAP1, 1 more genes
    nsv4985854copy number variation1nstd200human GRCh38 chr9: 135,871,662-135,871,857 , GRCh37.p13 chr9: 138,763,508-138,763,703 CAMSAP1
    nsv4985853copy number variation1nstd200human GRCh38 chr9: 135,865,734-135,958,903 , GRCh37.p13 chr9: 138,757,580-138,850,749 CAMSAP1, UBAC1, 1 more genes
    nsv4839443copy number variation1nstd200human GRCh37 chr9: 138,729,947-138,730,341 , GRCh38.p12 chr9: 135,838,101-135,838,495 CAMSAP1
    nsv4838493copy number variation1nstd200human GRCh37 chr9: 138,728,663-138,729,557 , GRCh38.p12 chr9: 135,836,817-135,837,711 CAMSAP1
    nsv4834695copy number variation1nstd200human GRCh37 chr9: 138,729,558-138,730,181 , GRCh38.p12 chr9: 135,837,712-135,838,335 CAMSAP1
    nsv4829955copy number variation1nstd200human GRCh37 chr9: 138,722,306-138,723,144 , GRCh38.p12 chr9: 135,830,460-135,831,298 CAMSAP1
    nsv4766219insertion1nstd199human GRCh37 chr9: 138,739,695-138,739,695 , GRCh38.p12 chr9: 135,847,849-135,847,849 CAMSAP1
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 TPRN, CCDC183, 137 more genes
    nsv4684240copy number variation1nstd102humanUncertain significance GRCh37 chr9: 137,880,493-138,781,516 , GRCh38.p12 chr9: 134,988,647-135,889,670 LINC01502, LOC107987040, 25 more genes
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