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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127058copy number variation1nstd186human GRCh37 chr17: 66,563,180-66,565,263 , GRCh38.p12 chr17: 68,567,039-68,569,122 , FAM20A
    nsv6126325copy number variation1nstd186human GRCh37 chr17: 66,548,806-66,549,121 , GRCh38.p12 chr17: 68,552,665-68,552,980 FAM20A
    nsv5943619copy number variation1nstd209human GRCh38 chr17: 68,567,037-68,569,118 , GRCh37.p13 chr17: 66,563,178-66,565,259 , FAM20A
    nsv5936722copy number variation1nstd209human GRCh38 chr17: 68,566,974-68,569,153 , GRCh37.p13 chr17: 66,563,115-66,565,294 , FAM20A
    nsv5931535copy number variation1nstd209human GRCh38 chr17: 68,552,650-68,552,979 , GRCh37.p13 chr17: 66,548,791-66,549,120 FAM20A
    nsv5928489copy number variation1nstd209human GRCh38 chr17: 68,571,939-68,572,002 , GRCh37.p13 chr17: 66,568,080-66,568,143 , FAM20A
    nsv5883513copy number variation1nstd209human GRCh38 chr17: 68,567,039-68,569,072 , GRCh37.p13 chr17: 66,563,180-66,565,213 , FAM20A
    nsv5672892copy number variation1nstd102humanPathogenic GRCh37 chr17: 66,508,520-66,533,875 , GRCh38.p12 chr17: 68,512,379-68,537,734 FAM20A, PRKAR1A
    nsv5589023copy number variation1nstd207human GRCh38 chr17: 68,571,939-68,571,996 , GRCh37.p13 chr17: 66,568,080-66,568,137 , FAM20A
    nsv5588712copy number variation1nstd207human GRCh38 chr17: 68,552,650-68,552,979 , GRCh37.p13 chr17: 66,548,791-66,549,120 FAM20A
    nsv5532253copy number variation1nstd206human GRCh38 chr17: 68,567,039-68,569,122 , GRCh37.p13 chr17: 66,563,180-66,565,263 , FAM20A
    nsv5525583copy number variation1nstd206human GRCh38 chr17: 68,552,665-68,552,980 , GRCh37.p13 chr17: 66,548,806-66,549,121 FAM20A
    nsv5522569copy number variation1nstd206human GRCh38 chr17: 68,581,447-68,581,567 , GRCh37.p13 chr17: 66,577,588-66,577,708 , FAM20A
    nsv5522302copy number variation1nstd206human GRCh38 chr17: 68,544,860-68,544,936 , GRCh37.p13 chr17: 66,541,001-66,541,077 PRKAR1A, FAM20A
    nsv5514290copy number variation1nstd206human GRCh38 chr17: 68,545,961-68,546,703 , GRCh37.p13 chr17: 66,542,102-66,542,844 PRKAR1A, FAM20A
    nsv5390236copy number variation2nstd186human GRCh37 chr17: 66,563,215-66,565,176 , GRCh38.p12 chr17: 68,567,074-68,569,035 , FAM20A
    nsv5383555mobile element deletion2nstd186human GRCh37 chr17: 66,548,806-66,549,121 , GRCh38.p12 chr17: 68,552,665-68,552,980 FAM20A
    nsv5349622translocation1nstd200human GRCh38 chr17: 68,544,936-68,544,936 , GRCh38 chr17: 68,544,860-68,544,860 , GRCh37.p13 chr17: 66,541,077-66,541,077 , GRCh37.p13 chr17: 66,541,001-66,541,001 FAM20A, PRKAR1A
    nsv5291638copy number variation1nstd204human GRCh38.p13 chr17: 68,552,701-68,553,000 , GRCh37.p13 chr17: 66,548,842-66,549,141 FAM20A
    nsv5200554mobile element deletion1nstd204human GRCh38.p13 chr17: 68,552,665-68,552,980 , GRCh37.p13 chr17: 66,548,806-66,549,121 FAM20A
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