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Items: 1 to 20 of 117

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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
    nsv7047897inversion1nstd229human GRCh38 chr7: 25,120,852-25,361,306 , GRCh37.p13 chr7: 25,160,471-25,400,925 RPL7AP41, LOC105375193, 7 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
    nsv6812782copy number variation1nstd229human GRCh38 chr7: 25,138,897-25,256,265 , GRCh37.p13 chr7: 25,178,516-25,295,884 RPL7AP41, NPVF, 2 more genes
    nsv6807417copy number variation1nstd229human GRCh38 chr7: 25,228,511-25,236,460 , GRCh37.p13 chr7: 25,268,130-25,276,079 NPVF
    nsv6803780copy number variation1nstd229human GRCh38 chr7: 24,875,875-25,258,607 , GRCh37.p13 chr7: 24,915,494-25,298,226 NPVF, SPMIP4, 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
    nsv6603061copy number variation1nstd223human GRCh38 chr7: 25,188,700-25,231,036 , GRCh37.p13 chr7: 25,228,319-25,270,655 LOC105375191, NPVF, 1 more genes
    nsv6574479inversion1nstd223human GRCh38 chr7: 25,224,251-25,236,893 , GRCh37.p13 chr7: 25,263,870-25,276,512 NPVF
    nsv6562499inversion1nstd223human GRCh38 chr7: 25,072,527-28,462,755 , GRCh37.p13 chr7: 25,112,146-28,502,373 HOXA10-AS, HOXA2, 72 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
    nsv6135756copy number variation1nstd213human GRCh37 chr7: 25,150,000-25,300,001 , GRCh38.p12 chr7: 25,110,381-25,260,382 CYCS, NPVF, 3 more genes
    nsv5682164mobile element insertion1nstd211human GRCh38 chr7: 25,228,800-25,228,800 , GRCh37.p13 chr7: 25,268,419-25,268,419 NPVF
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5370437translocation1nstd200human GRCh38 chr7: 25,224,262-25,224,262 , GRCh38 chr7: 25,246,297-25,246,297 , GRCh37.p13 chr7: 25,263,881-25,263,881 , GRCh37.p13 chr7: 25,285,916-25,285,916 NPVF
    nsv5370436translocation1nstd200human GRCh38 chr7: 25,224,251-25,224,251 , GRCh38 chr7: 25,236,893-25,236,893 , GRCh37.p13 chr7: 25,263,870-25,263,870 , GRCh37.p13 chr7: 25,276,512-25,276,512 NPVF
    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
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