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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054280inversion1nstd229human GRCh38 chr7: 128,104,928-130,077,832 , GRCh37.p13 chr7: 127,744,980-129,717,672 CICP14, RNA5SP243, 63 more genes
    nsv7047961inversion1nstd229human GRCh38 chr7: 123,155,784-130,261,366 , GRCh37.p13 chr7: 122,795,838-129,901,206 IQUB, LOC107986843, 122 more genes
    nsv7047247inversion1nstd229human GRCh38 chr7: 123,130,391-130,261,365 , GRCh37.p13 chr7: 122,770,445-129,901,205 RNA5SP244, RNA5SP243, 122 more genes
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 more genes
    nsv7043190inversion1nstd229human GRCh38 chr7: 123,472,699-130,834,800 , GRCh37.p13 chr7: 123,112,753-129,984,423 KCP, LINC01000, 138 more genes
    nsv6838086copy number variation1nstd229human GRCh38 chr7: 129,200,363-129,203,726 , GRCh37.p13 chr7: 128,840,204-128,843,567 SMO
    nsv6837835copy number variation1nstd229human GRCh38 chr7: 128,205,538-135,806,503 , GRCh37.p13 chr7: 127,845,591-135,491,251 RN7SL81P, IMP3P2, 155 more genes
    nsv6828081copy number variation1nstd229human GRCh38 chr7: 129,198,190-129,201,131 , GRCh37.p13 chr7: 128,838,031-128,840,972 SMO
    nsv6818727copy number variation1nstd229human GRCh38 chr7: 129,047,701-129,342,300 , GRCh37.p13 chr7: 128,687,755-128,982,141 RNY1P11, TSPAN33, 7 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
    nsv6566937inversion1nstd223human GRCh38 chr7: 129,196,844-129,197,471 , GRCh37.p13 chr7: 128,836,685-128,837,312 SMO
    nsv6433908copy number variation1nstd223human GRCh38 chr7: 129,201,157-129,201,821 , GRCh37.p13 chr7: 128,840,998-128,841,662 SMO
    nsv6433694copy number variation1nstd223human GRCh38 chr7: 129,197,689-129,201,949 , GRCh37.p13 chr7: 128,837,530-128,841,790 SMO
    nsv6429066copy number variation1nstd223human GRCh38 chr7: 129,200,363-129,203,722 , GRCh37.p13 chr7: 128,840,204-128,843,563 SMO
    nsv6418824copy number variation1nstd223human GRCh38 chr7: 129,195,984-129,196,868 , GRCh37.p13 chr7: 128,835,825-128,836,709 SMO
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313876copy number variation1nstd102humanPathogenic GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839 IMPDH1, SSU72L6, 174 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6313722copy number variation1nstd102humanPathogenic GRCh37 chr7: 123,967,475-132,729,981 , GRCh38.p12 chr7: 124,327,421-133,045,221 IRF5, MIR129-1, 153 more genes
    nsv6135962copy number variation1nstd213human GRCh37 chr7: 128,830,000-129,040,001 , GRCh38.p12 chr7: 129,190,159-129,400,160 SMO, AHCYL2, 2 more genes
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