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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146298insertion1nstd232human GRCh37.p13 chr7: 36,483,471-36,483,471 , GRCh38.p12 chr7: 36,443,862-36,443,862 ANLN
    nsv7046096inversion1nstd229human GRCh38 chr7: 36,434,804-36,496,749 , GRCh37.p13 chr7: 36,474,413-36,536,358 ANLN
    nsv7045806inversion1nstd229human GRCh38 chr7: 35,074,085-37,751,599 , GRCh37.p13 chr7: 35,113,697-37,791,201 RNU6-565P, SEPTIN7, 36 more genes
    nsv7045327inversion1nstd229human GRCh38 chr7: 34,817,999-37,653,204 , GRCh37.p13 chr7: 34,857,611-37,692,807 ELMO1-AS1, DPY19L2P1, 40 more genes
    nsv6833698copy number variation1nstd229human GRCh38 chr7: 36,413,503-36,414,847 , GRCh37.p13 chr7: 36,453,112-36,454,456 ANLN
    nsv6832328copy number variation1nstd229human GRCh38 chr7: 36,406,131-36,418,936 , GRCh37.p13 chr7: 36,445,740-36,458,545 ANLN
    nsv6821637copy number variation1nstd229human GRCh38 chr7: 36,428,626-36,428,873 , GRCh37.p13 chr7: 36,468,235-36,468,482 ANLN
    nsv6819912copy number variation1nstd229human GRCh38 chr7: 36,444,326-36,462,654 , GRCh37.p13 chr7: 36,483,935-36,502,263 ANLN
    nsv6636700copy number variation1nstd102humanUncertain significance GRCh37 chr7: 36,374,178-37,923,116 , GRCh38.p12 chr7: 36,334,569-37,883,514 GPR141, AOAH, 14 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
    nsv6617328copy number variation1nstd223human GRCh38 chr7: 36,401,612-36,402,281 , GRCh37.p13 chr7: 36,441,221-36,441,890 ANLN
    nsv6615486copy number variation1nstd223human GRCh38 chr7: 36,421,992-36,422,632 , GRCh37.p13 chr7: 36,461,601-36,462,241 ANLN
    nsv6614497copy number variation1nstd223human GRCh38 chr7: 36,401,590-36,403,912 , GRCh37.p13 chr7: 36,441,199-36,443,521 ANLN
    nsv6608921copy number variation1nstd223human GRCh38 chr7: 36,362,101-36,401,500 , GRCh37.p13 chr7: 36,401,710-36,441,109 MATCAP2, ANLN
    nsv6608210copy number variation1nstd223human GRCh38 chr7: 36,385,601-36,394,100 , GRCh37.p13 chr7: 36,425,210-36,433,709 ANLN, MATCAP2
    nsv6607728copy number variation1nstd223human GRCh38 chr7: 36,413,503-36,414,853 , GRCh37.p13 chr7: 36,453,112-36,454,462 ANLN
    nsv6604656copy number variation1nstd223human GRCh38 chr7: 36,445,162-36,447,440 , GRCh37.p13 chr7: 36,484,771-36,487,049 ANLN
    nsv6602302copy number variation1nstd223human GRCh38 chr7: 36,444,326-36,462,654 , GRCh37.p13 chr7: 36,483,935-36,502,263 ANLN
    nsv6600089copy number variation1nstd223human GRCh38 chr7: 36,389,301-36,390,100 , GRCh37.p13 chr7: 36,428,910-36,429,709 ANLN, MATCAP2
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
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