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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672778copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,096,088-112,105,696 , GRCh38.p12 chr11: 112,225,365-112,234,973 RPS6P16, PTS
    nsv6309034copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,097,157-112,104,288 , GRCh38.p12 chr11: 112,226,434-112,233,565 RPS6P16, PTS
    nsv4682086copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,097,167-112,104,278 , GRCh38.p12 chr11: 112,226,444-112,233,555 RPS6P16, PTS
    nsv6310446copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,001,426-13,004,353 , GRCh38.p12 chr19: 12,890,612-12,893,539 GCDH, RPS6P25
    nsv7095470copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,001,933-13,004,477 , GRCh38.p12 chr19: 12,891,119-12,893,663 RPS6P25, GCDH
    nsv7095638copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,001,933-13,003,258 , GRCh38.p12 chr19: 12,891,119-12,892,444 RPS6P25, GCDH
    nsv7093917copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,103,876-112,104,288 , GRCh38.p12 chr11: 112,233,153-112,233,565 RPS6P16, PTS
    nsv5673302copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 13,004,287-13,004,477 , GRCh38.p12 chr19: 12,893,473-12,893,663 GCDH, RPS6P25
    nsv3910625copy number variation1nstd102humanBenign GRCh38 chr3: 163,087,562-163,177,968 , GRCh37 chr3: 162,805,350-162,895,756 , NCBI36 chr3: 164,288,044-164,378,450 LINC01192, RPS6P4
    nsv3878673copy number variation1nstd102humanBenign GRCh37 chr2: 179,853,545-179,886,343 , GRCh38.p12 chr2: 178,988,818-179,021,616 RPS6P2, CCDC141
    nsv6314688copy number variation1nstd102humanLikely benign GRCh37 chr19: 13,004,474-13,004,533 , GRCh38 chr19: 12,893,660-12,893,719 RPS6P25, GCDH
    nsv4452590copy number variation1nstd102humanUncertain significance GRCh37 chr2: 179,853,544-179,946,111 , GRCh38.p12 chr2: 178,988,817-179,081,384 CCDC141, RPS6P2
    nsv6310618copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,996,012-13,004,373 , GRCh38.p12 chr19: 12,885,198-12,893,559 RPS6P25, KLF1, 1 more genes
    nsv6310282copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,004,287-13,008,687 , GRCh38.p12 chr19: 12,893,473-12,897,873 SYCE2, RPS6P25, 1 more genes
    nsv4683135copy number variation1nstd102humanPathogenic GRCh37 chr19: 13,004,385-13,008,073 , GRCh38 chr19: 12,893,571-12,897,259 GCDH, SYCE2, 1 more genes
    nsv3917088copy number variation1nstd102humanLikely benign NCBI36 chr3: 163,643,969-164,659,025 , GRCh37.p13 chr3: 162,161,275-163,176,331 , GRCh38.p12 chr3: 162,443,487-163,458,543 RPS6P4, LOC105374188, 2 more genes
    nsv3915137copy number variation1nstd102humanLikely benign NCBI36 chr3: 163,987,343-164,841,068 , GRCh37.p13 chr3: 162,504,649-163,358,374 , GRCh38.p12 chr3: 162,786,861-163,640,586 LOC105374188, RPS6P4, 2 more genes
    nsv3917484copy number variation1nstd102humanLikely benign NCBI36 chr3: 163,987,343-164,743,912 , GRCh37.p13 chr3: 162,504,649-163,261,218 , GRCh38.p12 chr3: 162,786,861-163,543,430 RNU7-82P, LINC01192, 2 more genes
    nsv3916491copy number variation1nstd102humanLikely benign NCBI36 chr3: 164,158,285-164,596,599 , GRCh37.p13 chr3: 162,675,591-163,113,905 , GRCh38.p12 chr3: 162,957,803-163,396,117 LOC105374188, LINC01192, 1 more genes
    nsv3906675copy number variation1nstd102humanBenign GRCh37 chr11: 112,068,593-112,108,776 , GRCh38.p12 chr11: 112,197,870-112,238,053 PTS, RPS6P16, 3 more genes
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