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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5915280copy number variation1nstd209human GRCh38 chr7: 90,498,904-90,590,027 , GRCh37.p13 chr7: 90,128,218-90,219,341 PTTG1IP2
    nsv5865021copy number variation1nstd209human GRCh38 chr7: 90,498,847-90,538,513 , GRCh37.p13 chr7: 90,128,161-90,167,827 PTTG1IP2
    nsv5681686mobile element insertion1nstd211human GRCh38 chr7: 90,489,567-90,489,567 , GRCh37.p13 chr7: 90,118,881-90,118,881 PTTG1IP2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5486240copy number variation1nstd206human GRCh38 chr7: 90,497,643-90,497,752 , GRCh37.p13 chr7: 90,126,957-90,127,066 PTTG1IP2
    nsv5485951copy number variation1nstd206human GRCh38 chr7: 90,497,443-90,505,890 , GRCh37.p13 chr7: 90,126,757-90,135,204 PTTG1IP2
    nsv5485291copy number variation1nstd206human GRCh38 chr7: 90,491,553-90,491,990 , GRCh37.p13 chr7: 90,120,867-90,121,304 PTTG1IP2
    nsv5484791copy number variation1nstd206human GRCh38 chr7: 90,441,521-90,477,958 , GRCh37.p13 chr7: 90,070,835-90,107,272 PTTG1IP2
    nsv5484693copy number variation1nstd206human GRCh38 chr7: 90,504,212-90,505,937 , GRCh37.p13 chr7: 90,133,526-90,135,251 PTTG1IP2
    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
    nsv5363951translocation1nstd200human GRCh38 chr7: 90,498,444-90,498,444 , GRCh38 chr7: 90,498,540-90,498,540 , GRCh37.p13 chr7: 90,127,758-90,127,758 , GRCh37.p13 chr7: 90,127,854-90,127,854 PTTG1IP2
    nsv5306922copy number variation1nstd204human GRCh38.p13 chr7: 90,441,517-90,477,952 , GRCh37.p13 chr7: 90,070,831-90,107,266 PTTG1IP2
    nsv5256033copy number variation1nstd204human GRCh38.p13 chr7: 90,441,412-90,478,051 , GRCh37.p13 chr7: 90,070,726-90,107,365 PTTG1IP2
    nsv5244984copy number variation1nstd204human GRCh38.p13 chr7: 90,487,301-90,491,100 , GRCh37.p13 chr7: 90,116,615-90,120,414 PTTG1IP2
    nsv5119576mobile element insertion1nstd203human GRCh38 chr7: 90,467,790-90,467,796 , GRCh37.p13 chr7: 90,097,104-90,097,110 PTTG1IP2
    nsv5117515mobile element insertion1nstd203human GRCh38 chr7: 90,496,190-90,496,203 , GRCh37.p13 chr7: 90,125,504-90,125,517 PTTG1IP2
    nsv5101326mobile element insertion1nstd203human GRCh38 chr7: 90,467,786-90,467,790 , GRCh37.p13 chr7: 90,097,100-90,097,104 PTTG1IP2
    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
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