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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5828343copy number variation1nstd209human GRCh37.p13 chr1|NW_003871055.3: 6,595,690-6,631,896 , GRCh38 chr1: 149,780,277-149,816,483 , GRCh37.p13 chr1: 149,751,833-149,788,037 FCGR1A, H2BC18, 1 more genes
    nsv5828226copy number variation1nstd209human GRCh38 chr1: 149,786,287-149,789,021 , GRCh37.p13 chr1: 149,757,843-149,760,577 , GRCh37.p13 chr1|NW_003871055.3: 6,601,700-6,604,434 FCGR1A, H2BC18
    nsv5431757copy number variation1nstd206human GRCh38 chr1: 149,784,587-149,802,587 , GRCh37.p13 chr1|NW_003871055.3: 6,600,000-6,618,000 , GRCh37.p13 chr1: 149,756,143-149,774,143 FCGR1A, H2BC18
    nsv5421806copy number variation1nstd206human GRCh38 chr1: 149,782,587-149,789,000 , GRCh37.p13 chr1|NW_003871055.3: 6,598,000-6,604,413 , GRCh37.p13 chr1: 149,754,143-149,760,556 H2BC18, FCGR1A
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4707631copy number variation1nstd195human GRCh37 chr1: 149,755,601-149,765,951 , GRCh38.p12 chr1: 149,784,045-149,794,395 FCGR1A, H2BC18
    nsv4703037copy number variation1nstd195human GRCh37 chr1: 149,748,351-149,754,501 , GRCh38.p12 chr1: 149,776,795-149,782,945 FCGR1A, H2BC18
    nsv4593940copy number variation1nstd183human GRCh37 chr1: 149,722,462-149,778,729 , GRCh38.p12 chr1: 149,750,912-149,807,173 FCGR1A, H2BC18, 2 more genes
    nsv4070547copy number variation1nstd166human GRCh37.p13 chr1: 149,763,279-149,764,171 , GRCh38.p12 chr1: 149,791,723-149,792,615 H2BC18, FCGR1A
    nsv4061274copy number variation1nstd166human GRCh37.p13 chr1: 149,754,000-149,771,000 , GRCh38.p12 chr1: 149,782,444-149,799,444 FCGR1A, H2BC18
    nsv4058070copy number variation1nstd166human GRCh37.p13 chr1: 149,751,000-149,793,000 , GRCh38.p12 chr1: 149,779,444-149,821,445 FCGR1A, H2BC18, 1 more genes
    nsv4057910copy number variation1nstd166human GRCh37.p13 chr1: 149,755,850-149,761,000 , GRCh38.p12 chr1: 149,784,294-149,789,444 FCGR1A, H2BC18
    nsv3960597copy number variation1nstd168human GRCh37.p13 chr1|NW_003871055.3: 6,536,437-6,595,909 , GRCh38 chr1: 149,721,024-149,780,496 , GRCh37.p13 chr1: 149,692,559-149,752,052 FCGR1A, LOC100129586, 4 more genes
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , CRB1, 1608 more genes
    nsv3889382copy number variation1nstd102humanBenign GRCh37 chr1: 149,754,410-149,763,756 , GRCh38.p12 chr1: 149,782,854-149,792,200 H2BC18, FCGR1A
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 , SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 , RNU1-153P, 4887 more genes
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