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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5970089inversion1nstd209human GRCh38 chr3: 127,777,672-127,779,072 , GRCh37.p13 chr3: 127,496,515-127,497,915 MGLL
    nsv5954169insertion1nstd209human GRCh38 chr3: 127,777,012-127,777,012 , GRCh37.p13 chr3: 127,495,855-127,495,855 MGLL
    nsv5902521copy number variation1nstd209human GRCh38 chr3: 127,694,311-127,694,382 , GRCh37.p13 chr3: 127,413,154-127,413,225 MGLL
    nsv5901782copy number variation1nstd209human GRCh38 chr3: 127,686,797-127,688,652 , GRCh37.p13 chr3: 127,405,640-127,407,495 MGLL
    nsv5888882copy number variation1nstd209human GRCh38 chr3: 127,810,847-127,811,263 , GRCh37.p13 chr3: 127,529,690-127,530,106 MGLL
    nsv5834644copy number variation1nstd209human GRCh38 chr3: 127,696,289-127,702,775 , GRCh37.p13 chr3: 127,415,132-127,421,618 MGLL
    nsv5834585copy number variation1nstd209human GRCh38 chr3: 127,696,739-127,697,838 , GRCh37.p13 chr3: 127,415,582-127,416,681 MGLL
    nsv5690371mobile element insertion2nstd211human GRCh38 chr3: 127,777,026-127,777,026 , GRCh37.p13 chr3: 127,495,869-127,495,869 MGLL
    nsv5621599insertion1nstd207human GRCh38 chr3: 127,777,671-127,777,671 , GRCh37.p13 chr3: 127,496,514-127,496,514 MGLL
    nsv5611052insertion1nstd207human GRCh38 chr3: 127,777,012-127,777,012 , GRCh37.p13 chr3: 127,495,855-127,495,855 MGLL
    nsv5580332copy number variation1nstd207human GRCh38 chr3: 127,694,311-127,694,382 , GRCh37.p13 chr3: 127,413,154-127,413,225 MGLL
    nsv5564746copy number variation1nstd207human GRCh38 chr3: 127,810,849-127,811,270 , GRCh37.p13 chr3: 127,529,692-127,530,113 MGLL
    nsv5560377sequence alteration1nstd206human GRCh38 chr3: 127,777,672-127,779,073 , GRCh37.p13 chr3: 127,496,515-127,497,916 MGLL
    nsv5551554insertion1nstd206human GRCh38 chr3: 127,777,673-127,777,673 , GRCh37.p13 chr3: 127,496,516-127,496,516 MGLL
    nsv5452518copy number variation1nstd206human GRCh38 chr3: 127,810,847-127,811,279 , GRCh37.p13 chr3: 127,529,690-127,530,122 MGLL
    nsv5451614copy number variation1nstd206human GRCh38 chr3: 127,742,554-127,743,566 , GRCh37.p13 chr3: 127,461,397-127,462,409 LOC107986127, MGLL
    nsv5451552copy number variation1nstd206human GRCh38 chr3: 127,785,218-127,786,448 , GRCh37.p13 chr3: 127,504,061-127,505,291 MGLL
    nsv5450867copy number variation1nstd206human GRCh38 chr3: 127,820,113-127,824,676 , GRCh37.p13 chr3: 127,538,956-127,543,519 MGLL
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