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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976053insertion1nstd209human GRCh38 chr12: 95,043,689-95,043,689 , GRCh37.p13 chr12: 95,437,465-95,437,465 NR2C1
    nsv5969302insertion1nstd209human GRCh38 chr12: 95,019,484-95,019,484 , GRCh37.p13 chr12: 95,413,260-95,413,260 NR2C1
    nsv5863200copy number variation1nstd209human GRCh38 chr12: 95,040,147-95,042,546 , GRCh37.p13 chr12: 95,433,923-95,436,322 NR2C1
    nsv5726596mobile element insertion1nstd211human GRCh38 chr12: 95,040,224-95,040,224 , GRCh37.p13 chr12: 95,434,000-95,434,000 NR2C1
    nsv5707609mobile element insertion1nstd211human GRCh38 chr12: 95,029,474-95,029,474 , GRCh37.p13 chr12: 95,423,250-95,423,250 NR2C1
    nsv5559162mobile element insertion1nstd206human GRCh38 chr12: 95,040,224-95,040,275 , GRCh37.p13 chr12: 95,434,000-95,434,051 NR2C1
    nsv5534480insertion1nstd206human GRCh38 chr12: 95,037,754-95,037,772 , GRCh37.p13 chr12: 95,431,530-95,431,548 NR2C1
    nsv5356282translocation1nstd200human GRCh38 chr12: 95,039,512-95,039,512 , GRCh38 chr12: 95,039,462-95,039,462 , GRCh37.p13 chr12: 95,433,288-95,433,288 , GRCh37.p13 chr12: 95,433,238-95,433,238 NR2C1
    nsv5313050copy number variation1nstd204human GRCh37.p13 chr12: 95,459,549-95,495,489 , GRCh38.p13 chr12: 95,065,773-95,101,713 , NR2C1, 2 more genes
    nsv5270747copy number variation1nstd204human GRCh38.p13 chr12: 95,065,801-95,101,600 , GRCh37.p13 chr12: 95,459,577-95,495,376 , NR2C1, 2 more genes
    nsv5267434copy number variation1nstd204human GRCh38.p13 chr12: 95,065,231-95,099,545 , GRCh37.p13 chr12: 95,459,007-95,493,321 , FGD6, 2 more genes
    nsv5126591mobile element insertion1nstd203human GRCh38 chr12: 95,049,777-95,049,793 , GRCh37.p13 chr12: 95,443,553-95,443,569 NR2C1
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4993580copy number variation1nstd200human GRCh38 chr12: 95,036,757-95,037,130 , GRCh37.p13 chr12: 95,430,533-95,430,906 NR2C1
    nsv4993579copy number variation1nstd200human GRCh38 chr12: 95,024,402-95,024,682 , GRCh37.p13 chr12: 95,418,178-95,418,458 NR2C1
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4844844copy number variation1nstd200human GRCh37 chr12: 95,418,178-95,418,458 , GRCh38.p12 chr12: 95,024,402-95,024,682 NR2C1
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
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