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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6606854copy number variation1nstd223human GRCh38 chr7: 41,684,210-41,684,744 , GRCh37.p13 chr7: 41,723,808-41,724,342 INHBA
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 LINC01447, ABCA13, 142 more genes
    nsv6312346copy number variation1nstd102humanPathogenic GRCh37 chr7: 39,726,267-42,262,852 , GRCh38.p12 chr7: 39,686,668-42,223,253 HMGN2P30, GLI3, 31 more genes
    nsv6136997copy number variation1nstd213human GRCh37 chr7: 41,470,000-42,060,001 , GRCh38.p12 chr7: 41,430,402-42,020,402 GLI3, INHBA, 5 more genes
    nsv6136995copy number variation1nstd213human GRCh37 chr7: 39,040,000-48,190,001 , GRCh38.p12 chr7: 39,000,400-48,150,404 ADCY1, AEBP1, 161 more genes
    nsv6135992copy number variation1nstd213human GRCh37 chr7: 39,290,000-48,200,001 , GRCh38.p12 chr7: 39,250,401-48,160,404 PSMA2, RALA, 160 more genes
    nsv6018963copy number variation1nstd212human GRCh38 chr7: 41,700,779-41,700,876 , GRCh37.p13 chr7: 41,740,377-41,740,474 INHBA, INHBA-AS1
    nsv5965206insertion1nstd209human GRCh38 chr7: 41,684,249-41,684,249 , GRCh37.p13 chr7: 41,723,847-41,723,847 INHBA
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381783copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969 ELK1P1, URGCP, 121 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4734743copy number variation1nstd199human GRCh37 chr7: 41,740,343-41,740,409 , GRCh38.p12 chr7: 41,700,745-41,700,811 INHBA, INHBA-AS1
    nsv4675195copy number variation1nstd102humanPathogenic GRCh37 chr7: 41,397,582-42,870,176 , GRCh38.p12 chr7: 41,357,984-42,830,577 LOC105375247, LOC107986787, 11 more genes
    nsv4498038mobile element insertion1nstd166human GRCh37.p13 chr7: 41,723,706-41,723,706 , GRCh38.p12 chr7: 41,684,108-41,684,108 INHBA, LOC107986789
    nsv4455279copy number variation1nstd102humanUncertain significance GRCh37 chr7: 40,198,215-43,252,984 , GRCh38.p12 chr7: 40,158,616-43,213,385 INHBA, LOC105375244, 34 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
    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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