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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053973inversion1nstd229human GRCh38 chr7: 123,822,142-126,067,712 , GRCh37.p13 chr7: 123,462,196-125,707,766 HYAL4, LOC101928211, 22 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
    nsv7043190inversion1nstd229human GRCh38 chr7: 123,472,699-130,834,800 , GRCh37.p13 chr7: 123,112,753-129,984,423 KCP, LINC01000, 138 more genes
    nsv7040901inversion1nstd229human GRCh38 chr7: 123,982,107-124,892,878 , GRCh37.p13 chr7: 123,622,161-124,532,932 LOC107986841, LOC105375483, 10 more genes
    nsv6835310copy number variation1nstd229human GRCh38 chr7: 124,178,382-124,342,093 , GRCh37.p13 chr7: 123,818,436-123,982,147 LOC105375484, LOC101928211, 1 more genes
    nsv6831540copy number variation1nstd229human GRCh38 chr7: 124,330,458-124,337,602 , GRCh37.p13 chr7: 123,970,512-123,977,656 LOC101928211, LOC107986841
    nsv6827522copy number variation1nstd229human GRCh38 chr7: 124,339,478-124,339,670 , GRCh37.p13 chr7: 123,979,532-123,979,724 LOC101928211, LOC107986841
    nsv6825992copy number variation1nstd229human GRCh38 chr7: 124,349,101-124,376,600 , GRCh37.p13 chr7: 123,989,155-124,016,654 LOC107986841, LOC101928211
    nsv6824405copy number variation1nstd229human GRCh38 chr7: 124,141,735-126,196,922 , GRCh37.p13 chr7: 123,781,789-125,836,976 LOC101928254, LOC100420864, 18 more genes
    nsv6824344copy number variation1nstd229human GRCh38 chr7: 124,344,528-124,344,855 , GRCh37.p13 chr7: 123,984,582-123,984,909 LOC107986841, LOC101928211
    nsv6636704copy number variation1nstd102humanUncertain significance GRCh37 chr7: 123,909,741-124,546,250 , GRCh38.p12 chr7: 124,269,687-124,906,196 LOC105375484, LOC101928211, 8 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
    nsv6612499copy number variation1nstd223human GRCh38 chr7: 124,141,544-124,409,327 , GRCh37.p13 chr7: 123,781,598-124,049,381 LOC101928211, LOC107986841, 2 more genes
    nsv6607646copy number variation1nstd223human GRCh38 chr7: 124,349,092-124,376,602 , GRCh37.p13 chr7: 123,989,146-124,016,656 LOC101928211, LOC107986841
    nsv6607620copy number variation1nstd223human GRCh38 chr7: 124,212,866-124,423,794 , GRCh37.p13 chr7: 123,852,920-124,063,848 LOC101928211, LOC102724577, 2 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6314995copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 114,885,745-124,728,629 , GRCh38.p12 chr7: 115,245,691-125,088,575 CAPZA2, CAV1, 109 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
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