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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6694481copy number variation1nstd229human GRCh38 chr2: 150,470,596-150,471,212 , GRCh37.p13 chr2: 151,327,110-151,327,726 RND3
    nsv6692524copy number variation1nstd229human GRCh38 chr2: 150,229,231-153,083,013 , GRCh37.p13 chr2: 151,085,745-153,939,527 RPL30P2, NEB, 30 more genes
    nsv6691520copy number variation1nstd229human GRCh38 chr2: 150,460,419-150,658,709 , GRCh37.p13 chr2: 151,316,933-151,515,223 RND3, LINC01920, 1 more genes
    nsv6689890copy number variation1nstd229human GRCh38 chr2: 150,356,801-150,733,700 , GRCh37.p13 chr2: 151,213,315-151,590,214 RND3, LOC105373685, 3 more genes
    nsv6687333copy number variation1nstd229human GRCh38 chr2: 149,993,003-150,470,951 , GRCh37.p13 chr2: 150,849,517-151,327,465 LINC01818, TRE-CTC9-1, 4 more genes
    nsv6682514copy number variation1nstd229human GRCh38 chr2: 150,460,525-150,497,038 , GRCh37.p13 chr2: 151,317,039-151,353,552 RND3
    nsv6680953copy number variation1nstd229human GRCh38 chr2: 150,487,574-150,490,031 , GRCh37.p13 chr2: 151,344,088-151,346,545 RND3
    nsv6680637copy number variation1nstd229human GRCh38 chr2: 150,270,737-150,811,974 , GRCh37.p13 chr2: 151,127,251-151,668,488 LINC01818, TRE-CTC9-1, 4 more genes
    nsv6541714inversion1nstd223human GRCh38 chr2: 148,865,353-155,671,569 , GRCh37.p13 chr2: 149,622,922-156,528,081 , LOC107985952, 79 more genes
    nsv6335792copy number variation1nstd223human GRCh38 chr2: 150,480,643-150,505,865 , GRCh37.p13 chr2: 151,337,157-151,362,379 RND3
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313481copy number variation1nstd102humanPathogenic GRCh37 chr2: 143,258,712-152,867,819 , GRCh38.p12 chr2: 142,501,143-152,011,305 STIP1P1, RNU6-715P, 98 more genes
    nsv6290982copy number variation1nstd102humanPathogenic GRCh37 chr2: 142,409,401-152,680,804 , GRCh38.p12 chr2: 141,651,832-151,824,290 LOC101928526, MTCO2P5, 101 more genes
    nsv6134500copy number variation1nstd213human GRCh37 chr2: 149,790,000-179,310,001 , GRCh38.p12 chr2: 148,934,069-178,445,274 , ACVR1, 394 more genes
    nsv5890791copy number variation1nstd209human GRCh38 chr2: 150,480,914-150,480,976 , GRCh37.p13 chr2: 151,337,428-151,337,490 RND3
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5450895copy number variation1nstd206human GRCh38 chr2: 141,459,078-156,842,302 , GRCh37.p13 chr2: 142,216,647-157,698,814 , LOC105373696, 163 more genes
    nsv5437309copy number variation1nstd206human GRCh38 chr2: 150,472,955-150,473,013 , GRCh37.p13 chr2: 151,329,469-151,329,527 RND3
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5381338copy number variation1nstd102humanPathogenic GRCh37 chr2: 136,473,383-152,727,396 , GRCh38.p12 chr2: 135,715,813-151,870,882 YY1P2, SPOPL, 156 more genes
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