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Items: 1 to 20 of 1948

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148227copy number variation1nstd102humanPathogenic GRCh38 chr14: 102,263,440-106,874,929 , GRCh37.p13 chr14: 102,729,777-107,283,138 TNFAIP2, IGHV4-30-2, 306 more genes
    nsv7137201copy number variation1nstd102humanPathogenic GRCh37 chr14: 103,636,647-107,285,437 , GRCh38.p12 chr14: 103,170,310-106,877,229 IGHD, IGH, 281 more genes
    nsv7099293copy number variation1nstd231human GRCh38.p12 chr14: 105,786,368-106,068,965 , GRCh37 chr14: 106,160,630-106,525,210 , GRCh38.p12 chr14|NT_187600.1: 162,062-475,851 IGH, IGHA1, 63 more genes
    nsv7074033inversion1nstd229human GRCh38 chr14: 105,916,823-106,025,143 , GRCh37.p13 chr14|NW_004166863.1: 579,990-688,310 IGHV7-4-1, IGHD1-1, 12 more genes
    nsv7071453inversion1nstd229human GRCh38 chr14: 104,922,043-106,758,290 , GRCh37.p13 chr14: 105,388,380-106,929,356 , GRCh37.p13 chr14|NW_004166863.1: 1-1,421,457 IGHD1-14, IGHVII-53-1, 206 more genes
    nsv7068661inversion1nstd229human GRCh38 chr14: 105,907,228-106,196,706 , GRCh37.p13 chr14|NW_004166863.1: 570,395-859,873 IGHV3-15, IGHV1-12, 39 more genes
    nsv6977258copy number variation1nstd229human GRCh38 chr14: 105,967,158-105,974,283 , GRCh37.p13 chr14|NW_004166863.1: 630,325-637,450 ADAM6, IGH
    nsv6976854copy number variation1nstd229human GRCh38 chr14: 105,864,197-106,005,096 , GRCh37.p13 chr14|NW_004166863.1: 527,364-668,263 IGHD2-2, IGHD1-14, 42 more genes
    nsv6975182copy number variation1nstd229human GRCh38 chr14: 105,864,198-105,986,582 , GRCh37.p13 chr14|NW_004166863.1: 527,365-649,749 IGHJ5, IGHD4-4, 39 more genes
    nsv6975044copy number variation1nstd229human GRCh38 chr14: 105,963,834-105,971,808 , GRCh37.p13 chr14|NW_004166863.1: 627,001-634,975 IGH, ADAM6
    nsv6973633copy number variation1nstd229human GRCh38 chr14: 105,891,709-105,986,575 , GRCh37.p13 chr14|NW_004166863.1: 554,876-649,742 IGHD1-7, IGHD6-19, 24 more genes
    nsv6973426copy number variation1nstd229human GRCh38 chr14: 105,864,263-106,037,965 , GRCh37.p13 chr14|NW_004166863.1: 527,430-701,132 IGHV2-5, IGHVIII-5-1, 46 more genes
    nsv6972711copy number variation1nstd229human GRCh38 chr14: 105,512,040-105,972,202 , GRCh37.p13 chr14: 105,999,340-106,320,043 IGHD6-6, IGHA1, 64 more genes
    nsv6972478copy number variation1nstd229human GRCh38 chr14: 105,863,240-106,622,360 , GRCh37.p13 chr14|NW_004166863.1: 526,407-1,285,527 IGHVII-15-1, IGHVIII-5-2, 137 more genes
    nsv6972090copy number variation1nstd229human GRCh38 chr14: 105,863,258-106,373,701 , GRCh37.p13 chr14|NW_004166863.1: 526,425-1,008,126 IGHD4-11, IGHD5-5, 99 more genes
    nsv6970152copy number variation1nstd229human GRCh38 chr14: 105,864,235-105,986,584 , GRCh37.p13 chr14|NW_004166863.1: 527,402-649,751 FAM30A, IGHVII-1-1, 39 more genes
    nsv6969658copy number variation1nstd229human GRCh38 chr14: 105,863,215-106,421,772 , GRCh37.p13 chr14|NW_004166863.1: 526,382-1,008,126 IGHD3-22, IGHD4-17, 106 more genes
    nsv6969310copy number variation1nstd229human GRCh38 chr14: 105,863,201-106,005,100 , GRCh37.p13 chr14|NW_004166863.1: 526,368-668,267 IGHVIII-2-1, RPS8P1, 44 more genes
    nsv6969166copy number variation1nstd229human GRCh38 chr14: 105,543,903-106,485,920 , GRCh37.p13 chr14: 106,010,240-106,929,356 , GRCh37.p13 chr14|NW_004166863.1: 236,423-1,025,122 MIR8071-1, IGHVII-15-1, 137 more genes
    nsv6967675copy number variation1nstd229human GRCh38 chr14: 105,863,257-106,622,360 , GRCh37.p13 chr14|NW_004166863.1: 526,424-1,285,527 IGHV3-54, IGHV3-50, 137 more genes
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