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Items: 1 to 20 of 964

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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
    nsv7143373insertion1nstd232human GRCh37.p13 chr14: 106,319,876-106,319,876 , GRCh38.p12 chr14: 105,853,544-105,853,544 , GRCh38.p12 chr14|NT_187600.1: 321,313-321,313 IGH, IGHM
    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
    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
    nsv7071156inversion1nstd229human GRCh38 chr14: 105,535,562-105,870,285 , GRCh37.p13 chr14: 106,001,899-106,320,043 MIR8071-1, IGHJ3, 32 more genes
    nsv6975811copy number variation1nstd229human GRCh38 chr14: 105,853,801-105,859,200 , GRCh37.p13 chr14|NW_004166863.1: 516,968-522,367 IGH, MIR4539, 4 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
    nsv6972289copy number variation1nstd229human GRCh38 chr14: 105,856,225-105,864,214 , GRCh37.p13 chr14|NW_004166863.1: 519,392-527,381 IGHJ1, MIR4507, 14 more genes
    nsv6971648copy number variation1nstd229human GRCh38 chr14: 105,852,256-105,854,403 , GRCh37.p13 chr14: 106,318,588-106,320,043 IGH, IGHM
    nsv6970842copy number variation1nstd229human GRCh38 chr14: 105,848,306-105,873,481 , GRCh37.p13 chr14|NW_004166863.1: 516,901-536,648 IGHJ3, IGHM, 14 more genes
    nsv6970822copy number variation1nstd229human GRCh38 chr14: 105,853,545-105,853,771 , GRCh37.p13 chr14: 106,319,877-106,320,043 IGH, IGHM
    nsv6970373copy number variation1nstd229human GRCh38 chr14: 105,746,551-105,860,185 , GRCh37.p13 chr14: 106,212,888-106,320,043 MIR4507, ATP6V1G1P1, 8 more genes
    nsv6969803copy number variation1nstd229human GRCh38 chr14: 105,708,664-105,863,198 , GRCh37.p13 chr14: 106,175,001-106,320,043 IGHJ2P, IGHJ4, 18 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
    nsv6968638copy number variation1nstd229human GRCh38 chr14: 105,773,880-105,860,182 , GRCh37.p13 chr14: 106,240,217-106,320,043 IGH, IGHD, 6 more genes
    nsv6967076copy number variation1nstd229human GRCh38 chr14: 105,708,667-105,864,214 , GRCh37.p13 chr14: 106,175,004-106,320,043 IGHD7-27, IGHD, 21 more genes
    nsv6966675copy number variation1nstd229human GRCh38 chr14: 105,808,945-105,935,830 , GRCh37.p13 chr14|NW_004166863.1: 516,901-598,997 MIR4539, IGHD, 42 more genes
    nsv6964696copy number variation1nstd229human GRCh38 chr14: 105,709,621-105,859,645 , GRCh37.p13 chr14: 106,175,958-106,320,043 IGHG3, ATP6V1G1P1, 10 more genes
    nsv6964103copy number variation1nstd229human GRCh38 chr14: 105,744,778-105,859,816 , GRCh37.p13 chr14: 106,211,115-106,320,043 MIR4538, MIR4537, 8 more genes
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