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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904462copy number variation1nstd209human GRCh38 chr2: 137,877,086-137,877,943 , GRCh37.p13 chr2: 138,634,656-138,635,513 LOC101928273
    nsv5889382copy number variation1nstd209human GRCh38 chr2: 137,889,187-137,889,304 , GRCh37.p13 chr2: 138,646,757-138,646,874 LOC101928273
    nsv5888881copy number variation1nstd209human GRCh38 chr2: 137,879,890-137,882,226 , GRCh37.p13 chr2: 138,637,460-138,639,796 LOC101928273
    nsv5831524copy number variation1nstd209human GRCh38 chr2: 137,879,804-137,882,277 , GRCh37.p13 chr2: 138,637,374-138,639,847 LOC101928273
    nsv5731026mobile element insertion1nstd211human GRCh38 chr2: 137,918,839-137,918,839 , GRCh37.p13 chr2: 138,676,409-138,676,409 LOC101928273
    nsv5682054mobile element insertion1nstd211human GRCh38 chr2: 137,885,758-137,885,758 , GRCh37.p13 chr2: 138,643,328-138,643,328 LOC101928273
    nsv5623863insertion1nstd207human GRCh38 chr2: 137,885,796-137,885,796 , GRCh37.p13 chr2: 138,643,366-138,643,366 LOC101928273
    nsv5610384insertion1nstd207human GRCh38 chr2: 137,923,745-137,923,745 , GRCh37.p13 chr2: 138,681,315-138,681,315 LOC101928273
    nsv5609925insertion1nstd207human GRCh38 chr2: 137,919,395-137,919,395 , GRCh37.p13 chr2: 138,676,965-138,676,965 LOC101928273
    nsv5583297copy number variation1nstd207human GRCh38 chr2: 137,911,409-137,911,647 , GRCh37.p13 chr2: 138,668,979-138,669,217 LOC101928273
    nsv5575682copy number variation1nstd207human GRCh38 chr2: 137,893,828-137,894,027 , GRCh37.p13 chr2: 138,651,398-138,651,597 LOC101928273
    nsv5570245copy number variation1nstd207human GRCh38 chr2: 137,892,555-137,894,025 , GRCh37.p13 chr2: 138,650,125-138,651,595 LOC101928273
    nsv5569104copy number variation1nstd207human GRCh38 chr2: 137,892,558-137,892,825 , GRCh37.p13 chr2: 138,650,128-138,650,395 LOC101928273
    nsv5566289copy number variation1nstd207human GRCh38 chr2: 137,893,950-137,894,031 , GRCh37.p13 chr2: 138,651,520-138,651,601 LOC101928273
    nsv5565551copy number variation1nstd207human GRCh38 chr2: 137,879,890-137,882,226 , GRCh37.p13 chr2: 138,637,460-138,639,796 LOC101928273
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5451841copy number variation1nstd206human GRCh38 chr2: 137,877,086-137,877,946 , GRCh37.p13 chr2: 138,634,656-138,635,516 LOC101928273
    nsv5436293copy number variation1nstd206human GRCh38 chr2: 137,879,893-137,882,227 , GRCh37.p13 chr2: 138,637,463-138,639,797 LOC101928273
    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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