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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3878548copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,091,967-197,113,811 , GRCh38 chr1: 197,122,837-197,144,681 ASPM, SEPTIN14P12
    nsv3888515copy number variation1nstd102humanBenign GRCh37 chr1: 197,099,068-197,112,094 , GRCh38.p12 chr1: 197,129,938-197,142,964 ASPM, SEPTIN14P12
    nsv3875059copy number variation1nstd102humanBenign GRCh37 chr1: 197,099,068-197,168,178 , GRCh38.p12 chr1: 197,129,938-197,199,048 ASPM, SEPTIN14P12, 1 more genes
    nsv4681287copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,053,444-197,447,595 , GRCh38.p12 chr1: 197,084,314-197,478,465 ASPM, CRB1, 4 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 ASPM, CRB1, 1608 more genes
    nsv3888143copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,413,479-201,764,737 , GRCh38.p12 chr1: 179,444,344-201,795,609 ASPM, CSRP1-AS1, 273 more genes
    nsv4673925copy number variation1nstd102humanPathogenic GRCh37 chr1: 177,551,193-199,599,056 , GRCh38.p12 chr1: 177,582,058-199,629,928 ASPM, QSOX1, 263 more genes
    nsv3878624copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,073,386-200,192,265 , GRCh38.p12 chr1: 179,104,251-200,223,137 ASPM, LOC105371661, 249 more genes
    nsv3905741copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,002,040-199,694,025 , NCBI36 chr1: 177,268,663-197,960,648 , GRCh38 chr1: 179,032,905-199,724,897 ASPM, SLC4A1APP2, 240 more genes
    nsv3877653copy number variation1nstd102humanPathogenic GRCh37 chr1: 179,011,314-199,022,759 , GRCh38.p12 chr1: 179,042,179-199,053,630 ASPM, LINC02818, 234 more genes
    nsv3897058copy number variation1nstd102humanPathogenic GRCh37 chr1: 189,003,614-199,584,994 , NCBI36 chr1: 187,270,237-197,851,617 , GRCh38 chr1: 189,034,483-199,615,866 ASPM, LINC02770, 89 more genes
    nsv6636303copy number variation1nstd102humanPathogenic GRCh37 chr1: 193,011,753-199,882,947 , GRCh38.p12 chr1: 193,042,623-199,913,819 ASPM, RPS2P9, 60 more genes
    nsv3902034copy number variation1nstd102humanPathogenic GRCh37 chr1: 195,483,439-197,865,624 , GRCh38 chr1: 195,514,309-197,896,494 , NCBI36 chr1: 193,750,062-196,132,247 ASPM, CFHR2, 24 more genes
    nsv5673314copy number variation1nstd102humanPathogenic GRCh37 chr1: 196,918,585-197,742,062 , GRCh38.p12 chr1: 196,949,455-197,772,932 ASPM, CFHR5, 11 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 ASPM, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 ASPM, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 ASPM, RNU1-153P, 4887 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 ASPM, LOC101060227, 1608 more genes
    nsv4450583copy number variation1nstd102humanPathogenic GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041 ASPM, RGS18, 1186 more genes
    nsv3881012copy number variation1nstd102humanPathogenic GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801 ASPM, LOC105372928, 1062 more genes
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