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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6692164copy number variation1nstd229human GRCh38 chr2: 142,173,482-145,423,511 , GRCh37.p13 chr2: 142,931,051-146,181,079 LOC100505498, MTCO2P5, 29 more genes
    nsv6691605copy number variation1nstd229human GRCh38 chr2: 136,115,914-144,517,285 , GRCh37.p13 chr2: 136,873,484-145,274,852 LOC105373652, LOC105373649, 68 more genes
    nsv6683722copy number variation1nstd229human GRCh38 chr2: 143,935,701-143,938,600 , GRCh37.p13 chr2: 144,693,268-144,696,167 LOC101928386
    nsv6348423copy number variation1nstd223human GRCh38 chr2: 143,819,034-144,199,529 , GRCh37.p13 chr2: 144,576,603-144,957,096 LOC101928386, GTDC1
    nsv6348370copy number variation1nstd223human GRCh38 chr2: 143,917,001-143,945,300 , GRCh37.p13 chr2: 144,674,568-144,702,867 LOC101928386, GTDC1
    nsv6346896copy number variation1nstd223human GRCh38 chr2: 143,948,236-143,948,797 , GRCh37.p13 chr2: 144,705,803-144,706,364 LOC101928386, GTDC1
    nsv6344527copy number variation1nstd223human GRCh38 chr2: 143,963,419-143,963,894 , GRCh37.p13 chr2: 144,720,986-144,721,461 GTDC1, LOC101928386
    nsv6339629copy number variation1nstd223human GRCh38 chr2: 143,928,701-143,936,300 , GRCh37.p13 chr2: 144,686,268-144,693,867 LOC101928386
    nsv6337289copy number variation1nstd223human GRCh38 chr2: 143,919,601-143,944,700 , GRCh37.p13 chr2: 144,677,168-144,702,267 LOC101928386, GTDC1
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 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
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 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
    nsv6243185mobile element insertion1nstd215human GRCh38 chr2: 143,958,908-143,958,908 , GRCh37.p13 chr2: 144,716,475-144,716,475 GTDC1, LOC101928386
    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
    nsv5437474copy number variation1nstd206human GRCh38 chr2: 143,950,481-143,950,558 , GRCh37.p13 chr2: 144,708,048-144,708,125 LOC101928386, GTDC1
    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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