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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922831copy number variation1nstd209human GRCh38 chr7: 23,194,631-23,194,957 , GRCh37.p13 chr7: 23,234,250-23,234,576 NUP42
    nsv5915586copy number variation1nstd209human GRCh38 chr7: 23,177,980-23,181,348 , GRCh37.p13 chr7: 23,217,599-23,220,967 NUP42, KLHL7
    nsv5911423copy number variation1nstd209human GRCh38 chr7: 23,187,899-23,187,950 , GRCh37.p13 chr7: 23,227,518-23,227,569 NUP42
    nsv5846455copy number variation1nstd209human GRCh38 chr7: 23,177,892-23,181,391 , GRCh37.p13 chr7: 23,217,511-23,221,010 KLHL7, NUP42
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5471812copy number variation1nstd206human GRCh38 chr7: 23,179,274-23,181,439 , GRCh37.p13 chr7: 23,218,893-23,221,058 NUP42
    nsv5118841mobile element insertion1nstd203human GRCh38 chr7: 23,182,363-23,182,365 , GRCh37.p13 chr7: 23,221,982-23,221,984 NUP42
    nsv5102668mobile element insertion1nstd203human GRCh38 chr7: 23,182,358-23,182,369 , GRCh37.p13 chr7: 23,221,977-23,221,988 NUP42
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4826863copy number variation1nstd200human GRCh37 chr7: 23,217,526-23,221,022 , GRCh38.p12 chr7: 23,177,907-23,181,403 NUP42, KLHL7
    nsv4679102copy number variation1nstd189human GRCh37.p13 chr7: 23,083,268-24,187,619 , GRCh38.p12 chr7: 23,043,649-24,148,000 CLK2P1, GPNMB, 24 more genes
    nsv4616618copy number variation1nstd183human GRCh37 chr7: 23,145,295-23,311,044 , GRCh38.p12 chr7: 23,105,676-23,271,425 GPNMB, NUP42, 4 more genes
    nsv4613679copy number variation1nstd183human GRCh37 chr7: 23,235,696-23,235,939 , GRCh38.p12 chr7: 23,196,077-23,196,320 NUP42
    nsv4600877copy number variation1nstd183human GRCh37 chr7: 23,234,191-23,234,547 , GRCh38.p12 chr7: 23,194,572-23,194,928 NUP42
    nsv4524712copy number variation1nstd166human GRCh37.p13 chr7: 23,217,533-23,220,984 , GRCh38.p12 chr7: 23,177,914-23,181,365 KLHL7, NUP42
    nsv4498319mobile element insertion1nstd166human GRCh37.p13 chr7: 23,221,977-23,221,977 , GRCh38.p12 chr7: 23,182,358-23,182,358 NUP42
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4435897copy number variation1nstd102humanPathogenic GRCh37 chr7: 23,236,782-30,690,453 , GRCh38.p12 chr7: 23,197,163-30,650,837 CCDC126, LOC389473, 138 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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