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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3134181copy number variation2nstd151human GRCh37 chr3: 118,870,068-118,870,144 , GRCh38.p12 chr3: 119,151,221-119,151,297 TEX55
    esv3039277copy number variation1estd209human GRCh37 chr3: 118,869,182-118,869,183 , GRCh38.p12 chr3: 119,150,335-119,150,336 TEX55
    esv2234632copy number variation1estd194human NCBI36 chr3: 120,351,873-120,351,874 , GRCh37.p13 chr3: 118,869,183-118,869,184 , GRCh38.p12 chr3: 119,150,336-119,150,337 TEX55
    esv1373740copy number variation1estd22human NCBI36 chr3: 120,351,878-120,351,879 , GRCh37.p13 chr3: 118,869,188-118,869,189 , GRCh38.p12 chr3: 119,150,341-119,150,342 TEX55
    nsv222471copy number variation1nstd6human NCBI35 chr3: 120,351,879-120,351,879 , GRCh37.p13 chr3: 118,869,189-118,869,189 , GRCh38.p12 chr3: 119,150,342-119,150,342 TEX55
    esv3245831insertion1estd209human GRCh37 chr3: 118,870,025-118,870,025 , GRCh38.p12 chr3: 119,151,178-119,151,178 TEX55
    esv2559667insertion1estd197human NCBI36 chr3: 120,352,715-120,352,715 , GRCh37.p13 chr3: 118,870,025-118,870,025 , GRCh38.p12 chr3: 119,151,178-119,151,178 TEX55
    esv2026781insertion1estd194human NCBI36 chr3: 120,352,716-120,352,716 , GRCh37.p13 chr3: 118,870,026-118,870,026 , GRCh38.p12 chr3: 119,151,179-119,151,179 TEX55
    nsv6712000copy number variation1nstd229human GRCh38 chr3: 119,145,555-119,149,898 , GRCh37.p13 chr3: 118,864,402-118,868,745 IGSF11, TEX55
    nsv6698786copy number variation1nstd229human GRCh38 chr3: 119,145,601-119,149,900 , GRCh37.p13 chr3: 118,864,448-118,868,747 TEX55, IGSF11
    nsv3122118copy number variation1nstd151human GRCh37 chr3: 118,870,068-118,909,956 , GRCh38.p12 chr3: 119,151,221-119,191,109 TEX55, UPK1B
    esv3039276copy number variation1estd209human GRCh37 chr3: 118,863,410-118,863,411 , GRCh38.p12 chr3: 119,144,563-119,144,564 IGSF11, TEX55
    esv2049339copy number variation1estd194human NCBI36 chr3: 120,346,101-120,346,102 , GRCh37.p13 chr3: 118,863,411-118,863,412 , GRCh38.p12 chr3: 119,144,564-119,144,565 IGSF11, TEX55
    nsv6712976copy number variation1nstd229human GRCh38 chr3: 119,083,999-119,153,674 , GRCh37.p13 chr3: 118,802,846-118,872,521 IGSF11, TEX55
    nsv4384904copy number variation1nstd173human GRCh37 chr3: 118,859,487-118,882,592 , GRCh38.p12 chr3: 119,140,640-119,163,745 IGSF11, TEX55
    nsv4406813copy number variation1nstd174human GRCh37 chr3: 118,718,361-118,863,770 , GRCh38.p12 chr3: 118,999,514-119,144,923 IGSF11, TEX55
    nsv3131281copy number variation1nstd151human GRCh37 chr3: 118,823,988-118,870,144 , GRCh38.p12 chr3: 119,105,141-119,151,297 IGSF11, TEX55
    esv3831829copy number variation10estd219human GRCh37 chr3: 118,718,361-118,863,770 , GRCh38.p12 chr3: 118,999,514-119,144,923 IGSF11, TEX55
    esv3597545copy number variation10estd214human GRCh37 chr3: 118,718,361-118,863,770 , GRCh38.p12 chr3: 118,999,514-119,144,923 TEX55, IGSF11
    esv2756586copy number variation1estd55human NCBI35 chr3: 120,171,301-120,346,688 , GRCh37.p13 chr3: 118,688,611-118,863,998 , GRCh38.p12 chr3: 118,969,764-119,145,151 IGSF11, TEX55
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