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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5492778copy number variation1nstd206human GRCh38 chr7: 90,228,329-90,228,431 , GRCh37.p13 chr7: 89,857,643-89,857,745 STEAP2
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5363948translocation1nstd200human GRCh38 chr7: 90,228,431-90,228,431 , GRCh38 chr7: 90,228,329-90,228,329 , GRCh37.p13 chr7: 89,857,745-89,857,745 , GRCh37.p13 chr7: 89,857,643-89,857,643 STEAP2
    nsv5107670mobile element insertion1nstd203human GRCh38 chr7: 90,217,347-90,217,363 , GRCh37.p13 chr7: 89,846,661-89,846,677 STEAP2
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4964946copy number variation1nstd200human GRCh38 chr7: 90,179,322-90,844,711 , GRCh37.p13 chr7: 89,808,636-90,474,026 , STEAP2-AS1, 12 more genes
    nsv4964931copy number variation1nstd200human GRCh38 chr7: 88,710,380-90,258,175 , GRCh37.p13 chr7: 88,339,694-89,887,489 RNU6-274P, TEX47, 10 more genes
    nsv4964929copy number variation1nstd200human GRCh38 chr7: 88,517,053-90,538,991 , GRCh37.p13 chr7: 88,146,368-90,168,305 , PTTG1IP2, 21 more genes
    nsv4950528copy number variation1nstd200human GRCh38 chr7: 88,494,048-90,880,305 , GRCh37.p13 chr7: 88,123,363-90,509,620 , LOC100419447, 25 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825141copy number variation1nstd200human GRCh37 chr7: 88,339,694-89,887,489 , GRCh38.p12 chr7: 88,710,380-90,258,175 LOC107986817, STEAP2, 10 more genes
    nsv4825139copy number variation1nstd200human GRCh37 chr7: 88,146,368-90,168,305 , GRCh38.p12 chr7: 88,517,053-90,538,991 , CFAP69, 21 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4706588copy number variation1nstd195human GRCh37 chr7: 89,834,101-89,988,601 , GRCh38.p12 chr7: 90,204,787-90,359,287 CFAP69, GTPBP10, 6 more genes
    nsv4684286copy number variation1nstd102humanUncertain significance GRCh37 chr7: 88,547,866-89,880,949 , GRCh38.p12 chr7: 88,918,552-90,251,635 RNU6-274P, STEAP2-AS1, 8 more genes
    nsv4684243copy number variation1nstd102humanUncertain significance GRCh37 chr7: 88,148,465-89,871,132 , GRCh38.p12 chr7: 88,519,150-90,241,818 STEAP2-AS1, DPY19L2P4, 12 more genes
    nsv4680927copy number variation1nstd189human GRCh37.p13 chr7: 88,340,149-89,886,317 , GRCh38.p12 chr7: 88,710,835-90,257,003 STEAP1, CFAP69, 10 more genes
    nsv4680837copy number variation1nstd189human GRCh37.p13 chr7: 88,113,722-89,885,076 , GRCh38.p12 chr7: 88,484,407-90,255,762 STEAP1, CFAP69, 15 more genes
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