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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046641inversion1nstd229human GRCh38 chr7: 26,933,019-27,296,129 , GRCh37.p13 chr7: 26,972,638-27,335,748 HOXA4, HOXA1, 23 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
    nsv7041351inversion1nstd229human GRCh38 chr7: 27,171,881-27,171,977 , GRCh37.p13 chr7: 27,211,500-27,211,596 HOXA10, HOXA10-AS, 1 more genes
    nsv6816875copy number variation1nstd229human GRCh38 chr7: 27,175,447-27,176,529 , GRCh37.p13 chr7: 27,215,066-27,216,148 HOXA10-HOXA9, HOXA10
    nsv6810294copy number variation1nstd229human GRCh38 chr7: 27,174,513-27,179,164 , GRCh37.p13 chr7: 27,214,132-27,218,783 HOXA10, HOXA11, 1 more genes
    nsv6802275copy number variation1nstd229human GRCh38 chr7: 27,165,111-27,169,645 , GRCh37.p13 chr7: 27,204,730-27,209,264 HOXA10-HOXA9, MIR196B, 3 more genes
    nsv6636445copy number variation1nstd102humanPathogenic GRCh37 chr7: 27,133,786-34,466,477 , GRCh38.p12 chr7: 27,094,167-34,426,865 MIR550A1, HOXA-AS3, 119 more genes
    nsv6636197copy number variation1nstd102humanUncertain significance GRCh37 chr7: 26,418,391-28,323,299 , GRCh38.p12 chr7: 26,378,771-28,283,680 LINC02860, LINC03095, 49 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
    nsv6611186copy number variation1nstd223human GRCh38 chr7: 27,136,039-27,383,176 , GRCh37.p13 chr7: 27,175,658-27,422,795 HOXA13, EVX1-AS, 17 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
    nsv6135915copy number variation1nstd213human GRCh37 chr7: 26,520,000-27,320,001 , GRCh38.p12 chr7: 26,480,380-27,280,382 EVX1, HOXA1, 30 more genes
    nsv5919512copy number variation1nstd209human GRCh38 chr7: 26,509,679-33,120,288 , GRCh37.p13 chr7: 26,549,298-33,159,900 , CPVL-AS1, 126 more genes
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 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
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
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