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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137083copy number variation1nstd102humanPathogenic GRCh38 chr17: 80,085,785-80,092,148 , GRCh37 chr17: 78,059,584-78,065,947 CCDC40
    nsv3887660copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,032,273-78,032,799 , GRCh38 chr17: 80,058,474-80,059,000 CCDC40
    nsv6310242copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,039,264-78,039,425 , GRCh38.p12 chr17: 80,065,465-80,065,626 CCDC40
    nsv6310241copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 78,021,971-78,024,070 , GRCh38.p12 chr17: 80,048,172-80,050,271 CCDC40
    nsv6137748copy number variation1nstd102humanLikely benign GRCh38 chr17: 80,090,254-80,090,346 , GRCh37 chr17: 78,064,053-78,064,145 CCDC40
    nsv6137695copy number variation1nstd102humanLikely benign GRCh37 chr17: 78,063,952-78,064,015 , GRCh38 chr17: 80,090,153-80,090,216 CCDC40
    nsv6137783copy number variation1nstd102humanBenign GRCh38 chr17: 80,090,387-80,090,449 , GRCh37 chr17: 78,064,186-78,064,248 CCDC40
    nsv5564160copy number variation1nstd102humanUncertain significance GRCh38 chr17: 80,090,269-80,090,354 , GRCh37 chr17: 78,064,068-78,064,153 CCDC40
    nsv4682775copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,059,782-78,069,270 , GRCh38.p12 chr17: 80,085,983-80,095,471 CCDC40
    nsv4457883copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,058,431-78,074,446 , GRCh38.p12 chr17: 80,084,632-80,100,647 CCDC40, GAA, 1 more genes
    nsv6310240copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,010,462-78,158,057 , GRCh38.p12 chr17: 80,036,663-80,184,258 CCDC40, GAA, 3 more genes
    nsv4457767copy number variation1nstd102humanUncertain significance GRCh37 chr17: 77,891,501-78,038,110 , GRCh38.p12 chr17: 79,917,702-80,064,311 CCDC40, TBC1D16, 2 more genes
    nsv6310339copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,032,273-78,163,691 , GRCh38.p12 chr17: 80,058,474-80,189,892 CCDC40, CARD14, 3 more genes
    nsv3889816copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,071,044-78,074,412 , GRCh38 chr17: 80,097,245-80,100,613 CCDC40, GAA, 1 more genes
    nsv5381256copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,071,024-78,073,594 , GRCh38.p12 chr17: 80,097,225-80,099,795 CCDC40, MIR1268B, 1 more genes
    nsv3886634copy number variation1nstd102humanUncertain significance GRCh38 chr17: 80,097,225-80,099,795 , GRCh37 chr17: 78,071,024-78,073,594 CCDC40, MIR1268B, 1 more genes
    nsv7095419copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,071,024-78,073,574 , GRCh38.p12 chr17: 80,097,225-80,099,775 CCDC40, GAA, 1 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 CCDC40, PRPSAP1, 1350 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 CCDC40, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 CCDC40, P4HB, 2366 more genes
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