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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049867inversion1nstd229human GRCh38 chr7: 23,516,897-26,099,511 , GRCh37.p13 chr7: 23,556,516-26,139,131 NPY, LINC03007, 34 more genes
    nsv7047344inversion1nstd229human GRCh38 chr7: 25,935,982-25,967,276 , GRCh37.p13 chr7: 25,975,602-26,006,896 MIR148A, LOC105375200, 1 more genes
    nsv7043886inversion1nstd229human GRCh38 chr7: 25,072,526-28,462,757 , GRCh37.p13 chr7: 25,112,145-28,502,375 HOXA3, CREB5, 72 more genes
    nsv7042130inversion1nstd229human GRCh38 chr7: 23,500,611-26,098,164 , GRCh37.p13 chr7: 23,540,230-26,137,784 CLK2P1, RNA5SP228, 34 more genes
    nsv6810011copy number variation1nstd229human GRCh38 chr7: 25,848,777-26,219,686 , GRCh37.p13 chr7: 25,888,397-26,259,306 LOC105375200, NFE2L3, 5 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6562499inversion1nstd223human GRCh38 chr7: 25,072,527-28,462,755 , GRCh37.p13 chr7: 25,112,146-28,502,373 HOXA10-AS, HOXA2, 72 more genes
    nsv6315453copy number variation1nstd102humanPathogenic GRCh37 chr7: 25,451,740-33,864,069 , GRCh38.p12 chr7: 25,412,121-33,824,457 PLEKHA8, NFE2L3, 141 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6135989copy number variation1nstd213human GRCh37 chr7: 25,680,000-28,100,001 , GRCh38.p12 chr7: 25,640,380-28,060,382 HOXA2, HOXA5, 58 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5370451translocation1nstd200human GRCh38 chr7: 25,949,892-25,949,892 , GRCh38 chr7: 25,945,279-25,945,279 , GRCh37.p13 chr7: 25,989,512-25,989,512 , GRCh37.p13 chr7: 25,984,899-25,984,899 MIR148A, LOC105375199, 1 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4956078copy number variation1nstd200human GRCh38 chr7: 25,950,066-25,953,059 , GRCh37.p13 chr7: 25,989,686-25,992,679 LOC105375199, MIR148A
    nsv4953510copy number variation1nstd200human GRCh38 chr7: 25,907,996-26,242,888 , GRCh37.p13 chr7: 25,947,616-26,282,508 MIR148A, LOC105375199, 5 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4729033copy number variation1nstd102humanUncertain significance GRCh37 chr7: 25,753,007-26,217,383 , GRCh38.p12 chr7: 25,713,387-26,177,763 NFE2L3, LINC03007, 5 more genes
    nsv4674822copy number variation1nstd102humanPathogenic GRCh37 chr7: 23,877,135-33,139,446 , GRCh38.p12 chr7: 23,837,516-33,099,834 RP9P, LINC00997, 156 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
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