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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907959copy number variation1nstd209human GRCh38 chr7: 79,468,045-79,468,095 , GRCh37.p13 chr7: 79,097,361-79,097,411 MAGI2-AS3
    nsv5866668copy number variation1nstd209human GRCh38 chr7: 79,451,844-79,454,122 , GRCh37.p13 chr7: 79,081,160-79,083,438 MAGI2, MAGI2-AS3
    nsv5724816mobile element insertion2nstd211human GRCh38 chr7: 79,466,925-79,466,925 , GRCh37.p13 chr7: 79,096,241-79,096,241 MAGI2-AS3
    nsv5688901mobile element insertion1nstd211human GRCh38 chr7: 79,465,518-79,465,518 , GRCh37.p13 chr7: 79,094,834-79,094,834 MAGI2-AS3
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5555062mobile element insertion1nstd206human GRCh38 chr7: 79,466,925-79,466,976 , GRCh37.p13 chr7: 79,096,241-79,096,292 MAGI2-AS3
    nsv5483451copy number variation1nstd206human GRCh38 chr7: 79,466,334-79,470,940 , GRCh37.p13 chr7: 79,095,650-79,100,256 MAGI2-AS3
    nsv5410436mobile element insertion1nstd206human GRCh38 chr7: 79,465,518-79,465,569 , GRCh37.p13 chr7: 79,094,834-79,094,885 MAGI2-AS3
    nsv5363871translocation1nstd200human GRCh38 chr7: 79,462,832-79,462,832 , GRCh38 chr7: 79,462,727-79,462,727 , GRCh37.p13 chr7: 79,092,043-79,092,043 , GRCh37.p13 chr7: 79,092,148-79,092,148 MAGI2-AS3
    nsv5107824mobile element insertion1nstd203human GRCh38 chr7: 79,459,286-79,459,286 , GRCh37.p13 chr7: 79,088,602-79,088,602 MAGI2-AS3
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4964864copy number variation1nstd200human GRCh38 chr7: 79,445,893-79,457,969 , GRCh37.p13 chr7: 79,075,209-79,087,285 MAGI2-AS3, MAGI2
    nsv4950215copy number variation1nstd200human GRCh38 chr7: 79,463,335-79,466,444 , GRCh37.p13 chr7: 79,092,651-79,095,760 MAGI2-AS3
    nsv4950214copy number variation1nstd200human GRCh38 chr7: 79,459,238-79,460,784 , GRCh37.p13 chr7: 79,088,554-79,090,100 MAGI2-AS3
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4680621copy number variation1nstd189human GRCh37.p13 chr7: 77,843,491-79,282,477 , GRCh38.p12 chr7: 78,214,174-79,653,161 MAGI2, RPL13AP17, 10 more genes
    nsv4599137copy number variation1nstd183human GRCh37 chr7: 79,094,787-79,099,849 , GRCh38.p12 chr7: 79,465,471-79,470,533 MAGI2-AS3
    nsv4563137mobile element insertion1nstd166human GRCh37.p13 chr7: 79,096,226-79,096,226 , GRCh38.p12 chr7: 79,466,910-79,466,910 MAGI2-AS3
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
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