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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3875806copy number variation1nstd102humanBenign GRCh37 chr6: 28,771,054-28,791,202 , GRCh38.p12 chr6: 28,803,277-28,823,425 TRA-TGC5-1, TRF-GAA3-1
    nsv3888118copy number variation1nstd102humanBenign GRCh37 chr6: 28,774,593-28,792,477 , GRCh38.p12 chr6: 28,806,816-28,824,700 TRF-GAA3-1, TRA-TGC5-1
    nsv3873601copy number variation1nstd102humanBenign GRCh37 chr6: 28,569,949-28,601,934 , GRCh38.p12 chr6: 28,602,172-28,634,157 TRA-AGC3-1, SCAND3, 1 more genes
    nsv3907698copy number variation1nstd102humanBenign GRCh37 chr14: 22,387,839-22,410,300 , GRCh38.p12 chr14: 21,919,664-21,942,109 TRA, TRAV14DV4, 1 more genes
    nsv3890818copy number variation1nstd102humanBenign GRCh37 chr11: 60,757,633-60,878,915 , GRCh38.p12 chr11: 60,990,161-61,111,443 LOC105369325, CD6, 3 more genes
    nsv3900042copy number variation1nstd102humanBenign GRCh37 chr11: 60,760,971-60,872,073 , GRCh38.p12 chr11: 60,993,499-61,104,601 LOC105369325, CD5, 3 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 TRA, HNRNPC, 616 more genes
    nsv3916277copy number variation1nstd102humanPathogenic NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005 TRA, MIR208B, 600 more genes
    nsv3898306copy number variation1nstd102humanPathogenic GRCh38 chr2: 148,917,286-163,204,623 , GRCh37 chr2: 149,674,855-164,061,133 , NCBI36 chr2: 149,391,325-163,769,379 RPS3AP13, LY75-CD302, 170 more genes
    nsv4674226copy number variation1nstd102humanPathogenic GRCh37 chr2: 147,173,792-158,346,266 , GRCh38.p12 chr2: 146,416,224-157,489,754 RBM43, LINC01931, 120 more genes
    nsv3902718copy number variation1nstd102humanPathogenic GRCh38 chr2: 147,251,948-157,856,378 , NCBI36 chr2: 147,725,986-158,421,136 , GRCh37 chr2: 148,009,516-158,712,890 RNU6-1275P, TRE-CTC9-1, 117 more genes
    nsv3921316copy number variation1nstd102humanPathogenic NCBI36 chr2: 155,624,215-165,414,901 , GRCh37.p13 chr2: 155,915,969-165,706,655 , GRCh38.p12 chr2: 155,059,457-164,850,145 LOC105373712, MTCO1P45, 121 more genes
    nsv3914999copy number variation1nstd102humanPathogenic NCBI36 chr12: 122,035,702-129,765,072 , GRCh38 chr12: 122,985,202-130,714,574 , GRCh37 chr12: 123,469,749-131,199,119 LINC00944, ATP6V0A2, 132 more genes
    nsv3894168copy number variation1nstd102humanPathogenic GRCh37 chr2: 152,788,858-160,276,245 , GRCh38 chr2: 151,932,344-159,419,734 , NCBI36 chr2: 152,497,104-159,984,491 RNU6-1001P, GSTM3P2, 88 more genes
    nsv3910092copy number variation1nstd102humanPathogenic NCBI36 chr2: 152,138,015-159,100,037 , GRCh37.p13 chr2: 152,429,769-159,391,791 , GRCh38.p12 chr2: 151,573,255-158,535,279 ACVR1C, LINC01876, 73 more genes
    nsv4455692copy number variation1nstd102humanPathogenic GRCh37 chr12: 122,169,403-129,084,163 , GRCh38.p12 chr12: 121,731,497-128,599,618 LOC107987176, LRRC43, 147 more genes
    nsv3923612copy number variation1nstd102humanPathogenic GRCh38 chr12: 120,718,786-127,500,215 , GRCh37 chr12: 121,156,589-127,984,760 , NCBI36 chr12: 119,640,972-126,550,713 NCOR2, LOC105378258, 161 more genes
    nsv1398443copy number variation1nstd102humanPathogenic GRCh37 chr5: 174,397,487-180,686,444 , GRCh38.p12 chr5: 174,970,484-181,259,443 TRV-AAC1-3, LOC105377762, 203 more genes
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