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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7097607copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 138,391,369-141,759,786 , GRCh38.p12 chr7: 138,706,624-142,059,986 LOC105375535, AGK-DT, 82 more genes
    nsv7057486inversion1nstd229human GRCh38 chr7: 141,032,956-142,024,053 , GRCh37.p13 chr7: 140,732,756-141,557,849 MGAM, LOC105375537, 26 more genes
    nsv7047243inversion1nstd229human GRCh38 chr7: 140,412,248-142,426,166 , GRCh37.p13 chr7: 140,112,048-142,048,195 OR9A4, AGK-DT, 69 more genes
    nsv7044890inversion1nstd229human GRCh38 chr7: 140,412,271-142,426,160 , GRCh37.p13 chr7: 140,112,071-142,048,195 WEE2, LOC105375535, 69 more genes
    nsv7040689inversion1nstd229human GRCh38 chr7: 140,412,886-142,426,274 , GRCh37.p13 chr7: 140,112,686-142,048,195 MYL6P4, TMEM178B, 69 more genes
    nsv6829144copy number variation1nstd229human GRCh38 chr7: 141,883,980-141,893,837 , GRCh37.p13 chr7|NW_003571040.1: 25,931-35,788 , GRCh37.p13 chr7: 141,583,780-141,593,637 OR9A1P
    nsv6819007copy number variation1nstd229human GRCh38 chr7: 141,886,577-141,886,737 , GRCh37.p13 chr7|NW_003571040.1: 28,528-28,688 , GRCh37.p13 chr7: 141,586,377-141,586,537 OR9A1P
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 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
    nsv6631839copy number variation1nstd224human GRCh37 chr7: 141,578,798-141,597,660 , GRCh38.p12 chr7: 141,878,998-141,897,860 OR9A1P
    nsv6425443copy number variation1nstd223human GRCh38 chr7: 141,862,204-141,886,080 , GRCh37.p13 chr7: 141,562,004-141,585,880 , GRCh37.p13 chr7|NW_003571040.1: 4,155-28,031 OR9A3P, OR9A1P
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6312322copy number variation1nstd102humanUncertain significance GRCh37 chr7: 137,761,265-141,759,786 , GRCh38.p12 chr7: 138,076,519-142,059,986 RPS17P12, RNU6-85P, 96 more genes
    nsv6291163copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,851,002-159,119,707 , GRCh38.p12 chr7: 134,166,250-159,327,017 TRB, ZC3HAV1L, 579 more genes
    nsv6290262copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,848,099-145,814,115 , GRCh38.p12 chr7: 134,163,347-146,117,023 TRBJ2-7, PRSS2, 341 more genes
    nsv6289885copy number variation1nstd102humanPathogenic GRCh37 chr7: 141,443,350-142,460,881 , GRCh38.p12 chr7: 141,743,550-142,732,123 , GRCh38.p12 chr7|NT_187562.1: 191,042-755,627 TAS2R4, OR9N1P, 95 more genes
    nsv6135567copy number variation1nstd213human GRCh37 chr7: 141,330,000-141,610,001 , GRCh38.p12 chr7: 141,630,200-141,910,201 TAS2R4, PRSS37, 17 more genes
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