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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148223copy number variation1nstd102humanPathogenic GRCh38 chr1: 61,077,177-62,865,614 , GRCh37.p13 chr1: 61,542,849-63,331,285 RPL13AP9, LOC105378768, 24 more genes
    nsv7099297copy number variation1nstd231human GRCh38.p12 chr1: 58,444,770-67,143,664 , GRCh37 chr1: 58,910,442-67,609,347 AK4, CYP2J2, 125 more genes
    nsv7099208copy number variation1nstd231human GRCh38.p12 chr1: 59,526,542-66,009,490 , GRCh37 chr1: 59,992,214-66,475,173 AK4, CYP2J2, 96 more genes
    nsv7095627copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,548,464-67,861,772 , GRCh38.p12 chr1: 61,082,792-67,396,089 ALG6, MIR3116-2, 94 more genes
    nsv7039143inversion1nstd229human GRCh38 chr1: 61,633,784-64,711,589 , GRCh37.p13 chr1: 62,099,456-65,177,272 MGC34796, RN7SL130P, 53 more genes
    nsv6652647copy number variation1nstd229human GRCh38 chr1: 61,647,742-61,653,850 , GRCh37.p13 chr1: 62,113,414-62,119,522 LOC107984964, MGC34796
    nsv6652635copy number variation1nstd229human GRCh38 chr1: 61,234,501-61,661,400 , GRCh37.p13 chr1: 61,700,173-62,127,072 NFIA-AS1, LOC107984964, 3 more genes
    nsv6636980copy number variation1nstd102humanUncertain significance GRCh37 chr1: 61,699,735-62,380,298 , GRCh38.p12 chr1: 61,234,063-61,914,626 LOC105378766, NFIA-AS1, 8 more genes
    nsv6335464copy number variation1nstd223human GRCh38 chr1: 61,648,801-61,653,800 , GRCh37.p13 chr1: 62,114,473-62,119,472 MGC34796, LOC107984964
    nsv6334967copy number variation1nstd223human GRCh38 chr1: 61,646,601-61,654,100 , GRCh37.p13 chr1: 62,112,273-62,119,772 MGC34796, LOC107984964
    nsv6334112copy number variation1nstd223human GRCh38 chr1: 61,607,901-61,673,700 , GRCh37.p13 chr1: 62,073,573-62,139,372 MGC34796, LOC107984964
    nsv6329921copy number variation1nstd223human GRCh38 chr1: 61,649,001-61,662,900 , GRCh37.p13 chr1: 62,114,673-62,128,572 LOC107984964, MGC34796
    nsv6328866copy number variation1nstd223human GRCh38 chr1: 61,646,701-61,659,400 , GRCh37.p13 chr1: 62,112,373-62,125,072 LOC107984964, MGC34796
    nsv6326192copy number variation1nstd223human GRCh38 chr1: 61,642,601-61,672,400 , GRCh37.p13 chr1: 62,108,273-62,138,072 MGC34796, LOC107984964
    nsv6323488copy number variation1nstd223human GRCh38 chr1: 61,648,701-61,664,100 , GRCh37.p13 chr1: 62,114,373-62,129,772 MGC34796, LOC107984964
    nsv6321268copy number variation1nstd223human GRCh38 chr1: 61,647,701-61,655,100 , GRCh37.p13 chr1: 62,113,373-62,120,772 MGC34796, LOC107984964
    nsv6318008copy number variation1nstd223human GRCh38 chr1: 61,618,001-61,661,400 , GRCh37.p13 chr1: 62,083,673-62,127,072 MGC34796, LOC107984964
    nsv6313485copy number variation1nstd102humanUncertain significance GRCh37 chr1: 61,699,736-62,125,970 , GRCh38.p12 chr1: 61,234,064-61,660,298 MGC34796, LOC105378766, 3 more genes
    nsv5984547copy number variation1nstd212human GRCh38 chr1: 61,647,741-61,653,848 , GRCh37.p13 chr1: 62,113,413-62,119,520 LOC107984964, MGC34796
    nsv5886414copy number variation1nstd209human GRCh38 chr1: 61,656,290-61,656,602 , GRCh37.p13 chr1: 62,121,962-62,122,274 MGC34796
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