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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4685996copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,799,615-35,808,850 , GRCh38.p12 chr9: 35,799,618-35,808,853 SPAG8, NPR2
    nsv3153003copy number variation1nstd151human GRCh37 chr9: 35,799,612-35,810,134 , GRCh38.p12 chr9: 35,799,615-35,810,137 SPAG8, NPR2
    nsv3155407copy number variation1nstd151human GRCh37 chr9: 35,800,703-35,810,555 , GRCh38.p12 chr9: 35,800,706-35,810,558 SPAG8, NPR2
    nsv3149974copy number variation1nstd151human GRCh37 chr9: 35,800,383-35,806,540 , GRCh38.p12 chr9: 35,800,386-35,806,543 SPAG8, NPR2
    nsv3142149copy number variation1nstd151human GRCh37 chr9: 35,800,383-35,806,235 , GRCh38.p12 chr9: 35,800,386-35,806,238 SPAG8, NPR2
    nsv3146197copy number variation1nstd151human GRCh37 chr9: 35,801,637-35,807,400 , GRCh38.p12 chr9: 35,801,640-35,807,403 SPAG8, NPR2
    nsv3139494copy number variation1nstd151human GRCh37 chr9: 35,807,324-35,810,311 , GRCh38.p12 chr9: 35,807,327-35,810,314 SPAG8, NPR2
    nsv3155992copy number variation1nstd151human GRCh37 chr9: 35,810,227-35,810,311 , GRCh38.p12 chr9: 35,810,230-35,810,314 SPAG8, NPR2
    esv3125284copy number variation1estd209human GRCh37 chr9: 35,807,401-35,807,410 , GRCh38.p12 chr9: 35,807,404-35,807,413 SPAG8, NPR2
    nsv937334copy number variation1nstd84human GRCh37 chr9: 35,811,819-35,812,515 , GRCh38.p12 chr9: 35,811,822-35,812,518 SPAG8, HINT2
    esv1001241copy number variation1estd180human NCBI36 chr9: 35,801,489-35,801,500 , GRCh37.p13 chr9: 35,811,489-35,811,500 , GRCh38.p12 chr9: 35,811,492-35,811,503 SPAG8, HINT2
    esv1446767copy number variation1estd22human NCBI36 chr9: 35,797,405-35,797,414 , GRCh37.p13 chr9: 35,807,405-35,807,414 , GRCh38.p12 chr9: 35,807,408-35,807,417 SPAG8, NPR2
    nsv3149723copy number variation1nstd151human GRCh37 chr9: 35,799,612-35,809,661 , GRCh38.p12 chr9: 35,799,615-35,809,664 SPAG8, NPR2
    nsv3140216copy number variation2nstd151human GRCh37 chr9: 35,800,016-35,808,855 , GRCh38.p12 chr9: 35,800,019-35,808,858 SPAG8, NPR2
    nsv3142209copy number variation1nstd151human GRCh37 chr9: 35,801,637-35,809,249 , GRCh38.p12 chr9: 35,801,640-35,809,252 SPAG8, NPR2
    nsv3140977copy number variation2nstd151human GRCh37 chr9: 35,799,612-35,806,540 , GRCh38.p12 chr9: 35,799,615-35,806,543 SPAG8, NPR2
    nsv3150702copy number variation1nstd151human GRCh37 chr9: 35,801,064-35,805,987 , GRCh38.p12 chr9: 35,801,067-35,805,990 SPAG8, NPR2
    nsv3156445copy number variation1nstd151human GRCh37 chr9: 35,807,017-35,810,311 , GRCh38.p12 chr9: 35,807,020-35,810,314 SPAG8, NPR2
    nsv959657copy number variation1nstd86human GRCh38.p12 chr9: 35,810,245-35,813,551 , GRCh37 chr9: 35,810,242-35,813,548 SPAG8, HINT2
    nsv5189056mobile element insertion1nstd203human GRCh38 chr9: 35,808,917-35,808,934 , GRCh37.p13 chr9: 35,808,914-35,808,931 SPAG8, NPR2
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