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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6837852copy number variation1nstd229human GRCh38 chr7: 40,975,401-40,983,300 , GRCh37.p13 chr7: 41,014,999-41,022,898 LINC01450
    nsv6836035copy number variation1nstd229human GRCh38 chr7: 40,965,001-40,994,600 , GRCh37.p13 chr7: 41,004,600-41,034,198 LINC01450
    nsv6831270copy number variation1nstd229human GRCh38 chr7: 40,969,601-40,974,300 , GRCh37.p13 chr7: 41,009,200-41,013,898 LINC01450
    nsv6830646copy number variation1nstd229human GRCh38 chr7: 39,656,501-41,139,000 , GRCh37.p13 chr7: 39,696,100-41,178,598 RALA, LOC105375242, 22 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
    nsv6603386copy number variation1nstd223human GRCh38 chr7: 40,979,929-40,982,435 , GRCh37.p13 chr7: 41,019,527-41,022,033 LINC01450
    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
    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
    nsv6136182copy number variation1nstd213human GRCh37 chr7: 40,690,000-41,140,001 , GRCh38.p12 chr7: 40,650,401-41,100,403 SUGCT, LINC01450, 4 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
    nsv6135765copy number variation1nstd213human GRCh37 chr7: 40,520,000-41,510,001 , GRCh38.p12 chr7: 40,480,401-41,470,403 LOC105375243, LOC105375246, 9 more genes
    nsv5965439insertion1nstd209human GRCh38 chr7: 40,968,011-40,968,011 , GRCh37.p13 chr7: 41,007,610-41,007,610 LINC01450
    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
    nsv4950030copy number variation1nstd200human GRCh38 chr7: 40,980,012-40,982,464 , GRCh37.p13 chr7: 41,019,610-41,022,062 LINC01450
    nsv4950029copy number variation1nstd200human GRCh38 chr7: 40,978,085-40,978,196 , GRCh37.p13 chr7: 41,017,683-41,017,794 LINC01450
    nsv4811439copy number variation1nstd200human GRCh37 chr7: 41,019,630-41,022,035 , GRCh38.p12 chr7: 40,980,032-40,982,437 LINC01450
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