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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060146inversion1nstd229human GRCh38 chr13: 70,704,220-75,002,513 , GRCh37.p13 chr13: 71,278,352-75,576,650 RNU4-10P, LOC107987191, 39 more genes
    nsv6957724copy number variation1nstd229human GRCh38 chr13: 74,400,301-74,404,900 , GRCh37.p13 chr13: 74,974,438-74,979,037 LOC105370259
    nsv6954947copy number variation1nstd229human GRCh38 chr13: 74,344,601-74,354,900 , GRCh37.p13 chr13: 74,918,738-74,929,037 LOC105370259
    nsv6954546copy number variation1nstd229human GRCh38 chr13: 74,288,371-74,300,041 , GRCh37.p13 chr13: 74,862,508-74,874,178 RNY1P5, LOC105370259
    nsv6952699copy number variation1nstd229human GRCh38 chr13: 74,385,452-74,385,585 , GRCh37.p13 chr13: 74,959,589-74,959,722 LOC105370259
    nsv6951323copy number variation1nstd229human GRCh38 chr13: 74,356,759-74,356,808 , GRCh37.p13 chr13: 74,930,896-74,930,945 LOC105370259
    nsv6950705copy number variation1nstd229human GRCh38 chr13: 74,394,492-74,396,884 , GRCh37.p13 chr13: 74,968,629-74,971,021 LOC105370259
    nsv6950037copy number variation1nstd229human GRCh38 chr13: 74,327,678-74,329,791 , GRCh37.p13 chr13: 74,901,815-74,903,928 LOC105370259
    nsv6948899copy number variation1nstd229human GRCh38 chr13: 72,025,801-74,742,700 , GRCh37.p13 chr13: 72,599,939-75,316,837 RNU6-66P, RNY1P8, 28 more genes
    nsv6948590copy number variation1nstd229human GRCh38 chr13: 74,358,742-74,358,950 , GRCh37.p13 chr13: 74,932,879-74,933,087 LOC105370259
    nsv6947694copy number variation1nstd229human GRCh38 chr13: 74,309,347-74,309,747 , GRCh37.p13 chr13: 74,883,484-74,883,884 LOC105370259
    nsv6944952copy number variation1nstd229human GRCh38 chr13: 74,377,986-74,385,075 , GRCh37.p13 chr13: 74,952,123-74,959,212 RPL21P108, LOC105370259
    nsv6943056copy number variation1nstd229human GRCh38 chr13: 74,286,701-74,289,200 , GRCh37.p13 chr13: 74,860,838-74,863,337 LOC105370259, RNY1P5
    nsv6943050copy number variation1nstd229human GRCh38 chr13: 74,348,901-74,352,600 , GRCh37.p13 chr13: 74,923,038-74,926,737 LOC105370259
    nsv6940870copy number variation1nstd229human GRCh38 chr13: 74,404,801-74,406,700 , GRCh37.p13 chr13: 74,978,938-74,980,837 LOC105370259
    nsv6940807copy number variation1nstd229human GRCh38 chr13: 74,296,746-74,296,955 , GRCh37.p13 chr13: 74,870,883-74,871,092 LOC105370259
    nsv6940100copy number variation1nstd229human GRCh38 chr13: 74,382,811-74,434,084 , GRCh37.p13 chr13: 74,956,948-75,008,221 LOC105370259, LINC00381, 1 more genes
    nsv6939578copy number variation1nstd229human GRCh38 chr13: 74,400,914-74,415,223 , GRCh37.p13 chr13: 74,975,051-74,989,360 LOC105370259, LOC100288208
    nsv6938951copy number variation1nstd229human GRCh38 chr13: 74,347,301-74,352,800 , GRCh37.p13 chr13: 74,921,438-74,926,937 LOC105370259
    nsv6637317copy number variation1nstd102humanUncertain significance GRCh37 chr13: 73,600,015-77,624,907 , GRCh38.p12 chr13: 73,025,877-77,050,772 LOC105370261, BTF3P11, 53 more genes
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