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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2662218copy number variation44estd199human GRCh37 chr7: 52,171,112-52,397,355 , GRCh38.p12 chr7: 52,103,416-52,329,659 LOC107986796
    esv2676574copy number variation189estd199human GRCh37 chr6: 78,967,194-79,036,497 , GRCh38.p12 chr6: 78,257,477-78,326,780 LOC105377865
    esv2670203copy number variation158estd199human GRCh37 chr6: 78,967,194-79,036,475 , GRCh38.p12 chr6: 78,257,477-78,326,758 LOC105377865
    esv2673452copy number variation28estd199human GRCh37 chr5: 97,047,855-97,096,158 , GRCh38.p12 chr5: 97,712,151-97,760,454 LOC391813
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2676981copy number variation78estd199human GRCh37 chr19: 41,345,203-41,375,827 , GRCh38.p12 chr19: 40,839,298-40,869,922 CYP2A6
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2674493copy number variation111estd199human GRCh37 chr1: 169,225,645-169,243,192 , GRCh38.p12 chr1: 169,256,407-169,273,954 NME7
    esv2669960copy number variation208estd199human GRCh37 chr9: 41,968,745-41,984,492 , GRCh38.p12 chr9: 39,823,727-39,839,474 FGF7P3
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2675135copy number variation79estd199human GRCh37 chr3: 53,027,148-53,038,898 , GRCh38.p12 chr3: 52,993,132-53,004,882 SFMBT1
    esv2668861copy number variation64estd199human GRCh37 chr9: 6,700,452-6,710,572 , GRCh38.p12 chr9: 6,700,452-6,710,572 LINC02851
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2677090copy number variation28estd199human GRCh37 chr9: 6,701,595-6,711,642 , GRCh38.p12 chr9: 6,701,595-6,711,642 LINC02851
    esv2675979copy number variation520estd199human GRCh37 chr6: 53,924,803-53,934,828 , GRCh38.p12 chr6: 54,060,005-54,070,030 MLIP
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2673043copy number variation328estd199human GRCh37 chr14: 80,106,288-80,115,049 , GRCh38.p12 chr14: 79,639,945-79,648,706 NRXN3
    esv2677597copy number variation57estd199human GRCh37 chr15: 100,414,545-100,422,992 , GRCh38.p12 chr15: 99,874,340-99,882,787 LOC400464
    esv2671335copy number variation339estd199human GRCh37 chr15: 91,981,577-91,989,265 , GRCh38.p12 chr15: 91,438,347-91,446,035 LOC107984778
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