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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3920790copy number variation1nstd102humanPathogenic GRCh38 chr3: 134,257,180-149,729,538 , NCBI36 chr3: 135,458,712-150,930,015 , GRCh37 chr3: 133,976,022-149,447,325 ARMC8, TFDP2, 203 more genes
    nsv3920279copy number variation1nstd102humanPathogenic GRCh38 chr3: 129,817,243-143,381,624 , GRCh37 chr3: 129,536,086-143,100,466 , NCBI36 chr3: 131,018,776-144,583,156 ARMC8, NPHP3-AS1, 218 more genes
    nsv3921297copy number variation1nstd102humanPathogenic NCBI36 chr3: 133,918,512-145,986,275 , GRCh38 chr3: 132,716,978-144,784,743 , GRCh37 chr3: 132,435,822-144,503,585 ARMC8, BFSP2, 169 more genes
    nsv3914757copy number variation1nstd102humanPathogenic NCBI36 chr3: 131,018,776-142,626,687 , GRCh38 chr3: 129,817,243-141,425,155 , GRCh37 chr3: 129,536,086-141,143,997 ARMC8, CLSTN2-AS1, 177 more genes
    nsv3921636copy number variation1nstd102humanPathogenic GRCh38 chr3: 135,227,451-145,870,770 , NCBI36 chr3: 136,428,983-147,071,247 , GRCh37 chr3: 134,946,293-145,588,557 ARMC8, A4GNT, 134 more genes
    nsv3918871copy number variation1nstd102humanPathogenic GRCh38 chr3: 130,401,265-139,005,019 , NCBI36 chr3: 131,602,799-140,206,551 , GRCh37 chr3: 130,120,109-138,723,861 ARMC8, FOXL2, 132 more genes
    nsv3910942copy number variation1nstd102humanPathogenic NCBI36 chr3: 135,535,085-142,902,990 , GRCh38 chr3: 134,333,553-141,701,458 , GRCh37 chr3: 134,052,395-141,420,300 ARMC8, MRAS, 96 more genes
    nsv3923685copy number variation1nstd102humanPathogenic GRCh37 chr3: 137,650,842-144,187,581 , NCBI36 chr3: 139,133,532-145,670,271 , GRCh38 chr3: 137,932,000-144,468,739 ARMC8, ATP1B3, 97 more genes
    nsv3915603copy number variation1nstd102humanPathogenic NCBI36 chr3: 139,192,655-144,820,318 , GRCh38 chr3: 137,991,123-143,618,786 , GRCh37 chr3: 137,709,965-143,337,628 ARMC8, NME9, 91 more genes
    nsv7096443copy number variation1nstd102humanPathogenic GRCh37 chr3: 137,781,658-138,665,815 , GRCh38.p12 chr3: 138,062,816-138,946,973 ARMC8, EEF1A1P25, 17 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 ARMC8, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 ARMC8, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 ARMC8, RPL23AP49, 2875 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 ARMC8, LINC02614, 1469 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 ARMC8, H1-10, 846 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 ARMC8, OR7E53P, 794 more genes
    nsv4347615copy number variation1nstd102humanPathogenic GRCh37 chr3: 135,288,025-146,874,012 , GRCh38.p12 chr3: 135,569,183-147,156,225 ARMC8, RPL6P9, 145 more genes
    nsv3889828copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 135,935,129-141,867,748 , GRCh38.p12 chr3: 136,216,287-142,148,906 ARMC8, ACTG1P1, 82 more genes
    nsv3920834copy number variation1nstd102humanUncertain significance NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931 ARMC8, NCK1-DT, 271 more genes
    nsv4451778copy number variation1nstd102humanUncertain significance GRCh37 chr3: 135,186,881-140,826,836 , GRCh38.p12 chr3: 135,468,039-141,107,994 ARMC8, EEF1A1P25, 73 more genes
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