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Items: 1 to 20 of 143

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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
    nsv7057176inversion1nstd229human GRCh38 chr7: 142,200,564-149,795,026 , GRCh37.p13 chr7: 141,988,816-149,492,114 RN7SL72P, RPL32P17, 258 more genes
    nsv7051735inversion1nstd229human GRCh38 chr7: 142,037,473-144,135,486 , GRCh37.p13 chr7: 141,988,816-143,832,579 LOC105375546, TRBV21-1, 162 more genes
    nsv7047519inversion1nstd229human GRCh38 chr7: 142,782,780-143,009,940 , GRCh37.p13 chr7: 142,490,590-142,707,027 TRBD2, TRPV6, 25 more genes
    nsv7046649inversion1nstd229human GRCh38 chr7: 142,280,484-143,114,495 , GRCh37.p13 chr7: 141,988,816-142,811,588 , GRCh37.p13 chr7|NW_003571040.1: 422,455-1,127,132 TRBJ2-1, TRBV7-6, 101 more genes
    nsv7038753inversion1nstd229human GRCh38 chr7: 142,885,811-143,104,873 , GRCh37.p13 chr7: 142,583,556-142,801,966 KEL, OR6W1P, 8 more genes
    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
    nsv6563275inversion1nstd223human GRCh38 chr7: 142,782,774-143,009,946 , GRCh37.p13 chr7: 142,490,584-142,707,033 , TRBV30, 26 more genes
    nsv6315433copy number variation1nstd102humanUncertain significance GRCh37 chr7: 141,937,588-142,716,850 , GRCh38.p12 chr7|NT_187562.1: 199,668-914,081 , GRCh38.p12 chr7: 142,288,582-143,019,763 TRBJ1-3, MTRNR2L6, 107 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 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
    nsv6135972copy number variation1nstd213human GRCh37 chr7: 142,120,000-143,090,001 , GRCh38.p12 chr7: 142,618,685-143,392,908 , GRCh38.p12 chr7|NT_187562.1: 622,348-1,111,570 , CASP2, 70 more genes
    nsv6135900copy number variation1nstd213human GRCh37 chr7: 142,330,000-143,440,001 , GRCh38.p12 chr7: 142,622,486-143,742,908 , EPHA1, 82 more genes
    nsv6135899copy number variation1nstd213human GRCh37 chr7: 142,330,000-143,270,001 , GRCh38.p12 chr7: 142,622,486-143,572,908 , GRCh38.p12 chr7|NT_187562.1: 626,148-1,111,570 , CLCN1, 80 more genes
    nsv6135568copy number variation1nstd213human GRCh37 chr7: 142,100,000-143,170,001 , GRCh38.p12 chr7: 142,618,685-143,472,908 , CASP2, 71 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
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