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Items: 1 to 20 of 1232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2667872copy number variation147estd199human GRCh37 chr1: 225,133,630-225,248,654 , GRCh38.p12 chr1: 224,945,928-225,060,952 DNAH14
    esv2678472copy number variation114estd199human GRCh37 chr14: 41,609,436-41,669,664 , GRCh38.p12 chr14: 41,140,233-41,200,461 LINC02315
    esv2665733copy number variation42estd199human GRCh37 chr9: 65,607,845-65,687,792 , GRCh38.p12 chr9: 67,268,943-67,319,293 CNTNAP3P2
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2666578copy number variation167estd199human GRCh37 chr17: 77,462,245-77,494,392 , GRCh38.p12 chr17: 79,466,163-79,498,310 RBFOX3
    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
    esv2678638copy number variation3estd199human GRCh37 chr14: 46,535,495-46,564,742 , GRCh38.p12 chr14: 46,066,292-46,095,539 LINC00871
    esv2662252copy number variation41estd199human GRCh37 chr16: 55,796,145-55,822,792 , GRCh38.p12 chr16: 55,762,233-55,788,880 CES1P1
    esv2669187copy number variation3estd199human GRCh37 chr13: 93,174,645-93,197,342 , GRCh38.p12 chr13: 92,522,392-92,545,089 GPC5
    esv2665317copy number variation65estd199human GRCh37 chr11: 7,811,173-7,833,378 , GRCh38.p12 chr11: 7,789,626-7,811,831 , GRCh38.p12 chr11|NT_187583.1: 10,494-32,699 , GRCh38.p12 chr11|NW_011332695.1: 10,494-32,701 OR5P2
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2660674copy number variation20estd199human GRCh37 chr18: 14,550,245-14,567,792 , GRCh38.p12 chr18: 14,550,246-14,567,793 LOC105372004
    esv2659504copy number variation6estd199human GRCh37 chr5: 41,226,813-41,243,961 , GRCh38.p12 chr5: 41,226,711-41,243,859 C6
    esv2670608copy number variation10estd199human GRCh37 chr18: 14,552,169-14,568,725 , GRCh38.p12 chr18: 14,552,170-14,568,726 LOC105372004
    esv2663733copy number variation2estd199human GRCh37 chr1: 241,355,369-241,370,912 , GRCh38.p12 chr1: 241,192,069-241,207,612 RGS7
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2664143copy number variation14estd199human GRCh37 chr10: 57,169,095-57,183,342 , GRCh38.p12 chr10: 55,409,335-55,423,582 PCDH15
    esv2666375copy number variation2estd199human GRCh37 chr9: 108,527,095-108,540,292 , GRCh38.p12 chr9: 105,764,814-105,778,011 TMEM38B
    esv2668294copy number variation22estd199human GRCh37 chr19: 12,164,726-12,177,597 , GRCh38.p12 chr19: 12,053,911-12,066,782 ZNF844
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