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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095423copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,618,104-79,674,270 , GRCh38.p12 chr17: 81,651,074-81,707,240 PDE6G, MRPL12, 5 more genes
    nsv7095371copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,618,104-79,894,690 , GRCh38.p12 chr17: 81,651,074-81,936,814 CCDC137, PPP1R27, 21 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv6996991copy number variation1nstd229human GRCh38 chr17: 81,663,501-81,669,300 , GRCh37.p13 chr17: 79,630,531-79,636,330 CCDC137, PDE6G, 1 more genes
    nsv6990442copy number variation1nstd229human GRCh38 chr17: 81,605,096-81,723,001 , GRCh37.p13 chr17: 79,572,122-79,690,031 CCDC137, TSPAN10, 8 more genes
    nsv6988565copy number variation1nstd229human GRCh38 chr17: 81,652,801-81,652,855 , GRCh37.p13 chr17: 79,619,831-79,619,885 PDE6G
    nsv6981340copy number variation1nstd229human GRCh38 chr17: 81,647,501-81,650,200 , GRCh37.p13 chr17: 79,614,527-79,617,230 PDE6G, TSPAN10
    nsv6980565copy number variation1nstd229human GRCh38 chr17: 81,636,424-81,659,686 , GRCh37.p13 chr17: 79,603,450-79,626,716 PDE6G, TSPAN10, 1 more genes
    nsv6530406copy number variation1nstd223human GRCh38 chr17: 81,650,201-81,651,700 , GRCh37.p13 chr17: 79,617,231-79,618,730 PDE6G
    nsv6527666copy number variation1nstd223human GRCh38 chr17: 81,663,534-81,667,396 , GRCh37.p13 chr17: 79,630,564-79,634,426 PDE6G, CCDC137, 1 more genes
    nsv6526209copy number variation1nstd223human GRCh38 chr17: 81,605,096-81,723,001 , GRCh37.p13 chr17: 79,572,122-79,690,031 HGS, SLC25A10, 8 more genes
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6274421copy number variation1nstd214human GRCh38 chr17: 81,652,798-81,652,850 , GRCh37.p13 chr17: 79,619,828-79,619,880 PDE6G
    nsv6133323copy number variation1nstd213human GRCh37 chr17: 78,760,000-81,195,210 , GRCh38.p12 chr17: 80,786,200-83,247,441 , ACTG1, 100 more genes
    nsv6032759copy number variation1nstd212human GRCh38 chr17: 81,652,798-81,652,851 , GRCh37.p13 chr17: 79,619,828-79,619,881 PDE6G
    nsv6023114copy number variation1nstd212human GRCh38 chr17: 81,663,426-81,663,727 , GRCh37.p13 chr17: 79,630,456-79,630,757 PDE6G, OXLD1
    nsv5938212copy number variation1nstd209human GRCh38 chr17: 81,652,798-81,652,850 , GRCh37.p13 chr17: 79,619,828-79,619,880 PDE6G
    nsv5595206copy number variation1nstd207human GRCh38 chr17: 81,652,798-81,652,850 , GRCh37.p13 chr17: 79,619,828-79,619,880 PDE6G
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