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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6717150copy number variation1nstd229human GRCh38 chr3: 121,563,091-121,569,237 , GRCh37.p13 chr3: 121,281,938-121,288,084 ARGFX
    nsv6701976copy number variation1nstd229human GRCh38 chr3: 121,578,824-121,582,995 , GRCh37.p13 chr3: 121,297,671-121,301,842 ARGFX
    nsv6707854copy number variation1nstd229human GRCh38 chr3: 121,576,224-121,578,587 , GRCh37.p13 chr3: 121,295,071-121,297,434 ARGFX
    nsv6701794copy number variation1nstd229human GRCh38 chr3: 121,575,082-121,575,582 , GRCh37.p13 chr3: 121,293,929-121,294,429 ARGFX
    nsv6368252copy number variation1nstd223human GRCh38 chr3: 121,563,091-121,569,232 , GRCh37.p13 chr3: 121,281,938-121,288,079 ARGFX
    nsv6374572copy number variation1nstd223human GRCh38 chr3: 121,578,817-121,582,989 , GRCh37.p13 chr3: 121,297,664-121,301,836 ARGFX
    nsv6361883copy number variation1nstd223human GRCh38 chr3: 121,576,887-121,579,971 , GRCh37.p13 chr3: 121,295,734-121,298,818 ARGFX
    nsv6365935copy number variation1nstd223human GRCh38 chr3: 121,576,224-121,578,587 , GRCh37.p13 chr3: 121,295,071-121,297,434 ARGFX
    nsv5434463copy number variation1nstd206human GRCh38 chr3: 121,584,970-121,585,059 , GRCh37.p13 chr3: 121,303,817-121,303,906 ARGFX
    nsv5991474copy number variation1nstd212human GRCh38 chr3: 121,583,545-121,583,627 , GRCh37.p13 chr3: 121,302,392-121,302,474 ARGFX
    nsv4919839copy number variation1nstd200human GRCh38 chr3: 121,578,824-121,582,989 , GRCh37.p13 chr3: 121,297,671-121,301,836 ARGFX
    nsv4806970copy number variation1nstd200human GRCh37 chr3: 121,297,668-121,301,837 , GRCh38.p12 chr3: 121,578,821-121,582,990 ARGFX
    nsv4806969copy number variation1nstd200human GRCh37 chr3: 121,295,650-121,298,902 , GRCh38.p12 chr3: 121,576,803-121,580,055 ARGFX
    nsv4919838copy number variation1nstd200human GRCh38 chr3: 121,576,886-121,579,972 , GRCh37.p13 chr3: 121,295,733-121,298,819 ARGFX
    nsv5890104copy number variation1nstd209human GRCh38 chr3: 121,578,252-121,580,728 , GRCh37.p13 chr3: 121,297,099-121,299,575 ARGFX
    nsv4919837copy number variation1nstd200human GRCh38 chr3: 121,576,224-121,578,587 , GRCh37.p13 chr3: 121,295,071-121,297,434 ARGFX
    nsv4806968copy number variation1nstd200human GRCh37 chr3: 121,295,071-121,297,434 , GRCh38.p12 chr3: 121,576,224-121,578,587 ARGFX
    nsv4919836copy number variation1nstd200human GRCh38 chr3: 121,565,709-121,567,071 , GRCh37.p13 chr3: 121,284,556-121,285,918 ARGFX
    nsv4919840copy number variation1nstd200human GRCh38 chr3: 121,588,671-121,588,790 , GRCh37.p13 chr3: 121,307,518-121,307,637 ARGFX
    nsv4806972copy number variation1nstd200human GRCh37 chr3: 121,307,518-121,307,637 , GRCh38.p12 chr3: 121,588,671-121,588,790 ARGFX
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