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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6831956copy number variation1nstd229human GRCh38 chr7: 87,850,747-87,946,783 , GRCh37.p13 chr7: 87,480,062-87,576,098 ADAM22, SLC25A40, 1 more genes
    nsv6831557copy number variation1nstd229human GRCh38 chr7: 87,870,584-87,979,300 , GRCh37.p13 chr7: 87,499,899-87,608,615 ADAM22, SLC25A40, 1 more genes
    nsv6831047copy number variation1nstd229human GRCh38 chr7: 87,835,642-88,074,696 , GRCh37.p13 chr7: 87,464,957-87,704,011 ADAM22, SLC25A40, 1 more genes
    nsv6830503copy number variation1nstd229human GRCh38 chr7: 87,902,901-87,906,300 , GRCh37.p13 chr7: 87,532,216-87,535,615 DBF4
    nsv6829401copy number variation1nstd229human GRCh38 chr7: 87,883,622-87,931,535 , GRCh37.p13 chr7: 87,512,937-87,560,850 DBF4
    nsv6826906copy number variation1nstd229human GRCh38 chr7: 87,888,601-87,893,600 , GRCh37.p13 chr7: 87,517,916-87,522,915 DBF4
    nsv6821564copy number variation1nstd229human GRCh38 chr7: 87,854,601-87,882,300 , GRCh37.p13 chr7: 87,483,916-87,511,615 SLC25A40, DBF4
    nsv6819583copy number variation1nstd229human GRCh38 chr7: 87,866,897-87,875,066 , GRCh37.p13 chr7: 87,496,212-87,504,381 SLC25A40, DBF4
    nsv6818739copy number variation1nstd229human GRCh38 chr7: 84,598,855-91,861,148 , GRCh37.p13 chr7: 84,228,171-91,490,462 CDK14, LOC101409256, 59 more genes
    nsv6636368copy number variation1nstd102humanUncertain significance GRCh37 chr7: 87,379,070-87,880,398 , GRCh38.p12 chr7: 87,749,754-88,251,083 SRI, LOC105375386, 5 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
    nsv6632462copy number variation1nstd224human GRCh37 chr7: 86,944,642-87,517,349 , GRCh38.p12 chr7: 87,315,326-87,888,034 ABCB1, ABCB4, 6 more genes
    nsv6632272copy number variation1nstd224human GRCh37 chr7: 87,476,339-87,514,832 , GRCh38.p12 chr7: 87,847,024-87,885,517 SLC25A40, DBF4
    nsv6619794copy number variation1nstd223human GRCh38 chr7: 87,908,952-87,909,936 , GRCh37.p13 chr7: 87,538,267-87,539,251 DBF4
    nsv6609852copy number variation1nstd223human GRCh38 chr7: 87,871,601-87,876,900 , GRCh37.p13 chr7: 87,500,916-87,506,215 SLC25A40, DBF4
    nsv6572644inversion1nstd223human GRCh38 chr7: 87,888,694-87,889,781 , GRCh37.p13 chr7: 87,518,009-87,519,096 DBF4
    nsv6563144inversion1nstd223human GRCh38 chr7: 87,903,993-87,904,737 , GRCh37.p13 chr7: 87,533,308-87,534,052 DBF4
    nsv6562151inversion1nstd223human GRCh38 chr7: 87,897,787-87,898,796 , GRCh37.p13 chr7: 87,527,102-87,528,111 DBF4
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313801copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825 SOCS5P1, FAM133B, 140 more genes
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