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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5679728mobile element insertion1nstd211human GRCh38 chr7: 90,395,745-90,395,745 , GRCh37.p13 chr7: 90,025,059-90,025,059 , LOC101409256
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5412434mobile element insertion1nstd206human GRCh38 chr7: 90,395,695-90,395,745 , GRCh37.p13 chr7: 90,025,009-90,025,059 , LOC101409256
    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
    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
    nsv4964947copy number variation1nstd200human GRCh38 chr7: 90,360,933-90,429,620 , GRCh37.p13 chr7: 89,990,247-90,058,934 , CLDN12, 2 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
    nsv4964929copy number variation1nstd200human GRCh38 chr7: 88,517,053-90,538,991 , GRCh37.p13 chr7: 88,146,368-90,168,305 , PTTG1IP2, 21 more genes
    nsv4950588copy number variation1nstd200human GRCh38 chr7: 90,392,882-90,395,372 , GRCh37.p13 chr7: 90,022,196-90,024,686 , LOC101409256
    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
    nsv4825154copy number variation1nstd200human GRCh37 chr7: 89,990,247-90,058,934 , GRCh38.p12 chr7: 90,360,933-90,429,620 , LOC101409256, 2 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
    nsv4819522copy number variation1nstd200human GRCh37 chr7: 90,022,234-90,024,649 , GRCh38.p12 chr7: 90,392,920-90,395,335 , LOC101409256
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4679378copy number variation1nstd189human GRCh37.p13 chr7: 89,693,737-90,284,958 , GRCh38.p12 chr7: 90,064,423-90,655,644 , CDK14, 14 more genes
    nsv4675401copy number variation1nstd102humanUncertain significance GRCh37 chr7: 88,533,008-90,192,559 , GRCh38.p12 chr7: 88,903,694-90,563,245 LOC101927446, GTPBP10, 15 more genes
    nsv4611127copy number variation1nstd183human GRCh37 chr7: 89,812,643-90,193,186 , GRCh38.p12 chr7: 90,183,329-90,563,872 , LOC101409256, 10 more genes
    nsv4606558copy number variation1nstd183human GRCh37 chr7: 90,019,904-90,067,714 , GRCh38.p12 chr7: 90,390,590-90,438,400 , CLDN12, 2 more genes
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