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Items: 1 to 20 of 289

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945718copy number variation1nstd209human GRCh38 chr13: 106,496,336-106,496,408 , GRCh37.p13 chr13: 107,148,684-107,148,756 EFNB2
    nsv5931669copy number variation1nstd209human GRCh38 chr13: 106,510,589-106,510,775 , GRCh37.p13 chr13: 107,162,937-107,163,123 EFNB2
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5513455copy number variation1nstd206human GRCh38 chr13: 106,505,523-106,505,663 , GRCh37.p13 chr13: 107,157,871-107,158,011 EFNB2
    nsv5508196copy number variation1nstd206human GRCh38 chr13: 106,496,338-106,496,409 , GRCh37.p13 chr13: 107,148,686-107,148,757 EFNB2
    nsv5504274copy number variation1nstd206human GRCh38 chr13: 106,510,590-106,510,776 , GRCh37.p13 chr13: 107,162,938-107,163,124 EFNB2
    nsv5497062copy number variation1nstd206human GRCh38 chr13: 106,126,808-107,477,062 , GRCh37.p13 chr13: 106,779,157-108,129,410 , RPL35P7, 18 more genes
    nsv5348939translocation1nstd200human GRCh38 chr13: 106,510,776-106,510,776 , GRCh38 chr13: 106,510,590-106,510,590 , GRCh37.p13 chr13: 107,162,938-107,162,938 , GRCh37.p13 chr13: 107,163,124-107,163,124 EFNB2
    nsv5342375translocation1nstd200human GRCh37 chr13: 107,162,938-107,162,938 , GRCh37 chr13: 107,163,124-107,163,124 , GRCh38.p12 chr13: 106,510,776-106,510,776 , GRCh38.p12 chr13: 106,510,590-106,510,590 EFNB2
    nsv5319652copy number variation1nstd204human GRCh38.p13 chr13: 106,510,566-106,510,798 , GRCh37.p13 chr13: 107,162,914-107,163,146 EFNB2
    nsv5144973mobile element insertion1nstd203human GRCh38 chr13: 106,521,146-106,521,161 , GRCh37.p13 chr13: 107,173,494-107,173,509 EFNB2
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4845409copy number variation1nstd200human GRCh37 chr13: 107,149,607-107,150,244 , GRCh38.p12 chr13: 106,497,259-106,497,896 EFNB2
    nsv4728884copy number variation1nstd102humanPathogenic GRCh37 chr13: 106,256,198-115,107,733 , GRCh38.p12 chr13: 105,603,849-114,342,258 LINC01044, CARS2, 139 more genes
    nsv4728419copy number variation1nstd102humanPathogenic GRCh37 chr13: 102,175,801-115,169,858 , GRCh38.p12 chr13: 101,523,450-114,344,403 RPL7P45, LOC107984615, 182 more genes
    nsv4675882copy number variation1nstd102humanPathogenic GRCh37 chr13: 104,521,177-109,327,788 , GRCh38.p12 chr13: 103,868,827-108,604,133 LOC107984608, LOC105370353, 39 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4675644copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258 ZIC2, LINC03032, 266 more genes
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