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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099298copy number variation1nstd231human GRCh38.p12 chr1: 68,115,402-81,183,740 , GRCh37 chr1: 68,581,085-81,649,425 ACADM, COX6A1P1, 145 more genes
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7053291inversion1nstd229human GRCh38 chr1: 77,170,361-77,177,341 , GRCh37.p13 chr1: 77,636,046-77,643,026 PIGK
    nsv7052065inversion1nstd229human GRCh38 chr1: 77,173,049-77,176,620 , GRCh37.p13 chr1: 77,638,734-77,642,305 PIGK
    nsv7047632inversion1nstd229human GRCh38 chr1: 74,160,663-78,762,216 , GRCh37.p13 chr1: 74,626,347-79,227,901 SLC44A5, MGC27382, 66 more genes
    nsv6655202copy number variation1nstd229human GRCh38 chr1: 77,196,001-77,196,900 , GRCh37.p13 chr1: 77,661,686-77,662,585 PIGK
    nsv6655201copy number variation1nstd229human GRCh38 chr1: 77,189,832-77,201,121 , GRCh37.p13 chr1: 77,655,517-77,666,806 PIGK, LOC100421400
    nsv6655200copy number variation1nstd229human GRCh38 chr1: 77,164,191-77,176,577 , GRCh37.p13 chr1: 77,629,876-77,642,262 PIGK
    nsv6655199copy number variation1nstd229human GRCh38 chr1: 77,119,008-77,119,061 , GRCh37.p13 chr1: 77,584,693-77,584,746 PIGK
    nsv6655198copy number variation1nstd229human GRCh38 chr1: 77,093,984-77,098,946 , GRCh37.p13 chr1: 77,559,669-77,564,631 PIGK
    nsv6655124copy number variation1nstd229human GRCh38 chr1: 77,155,254-77,163,700 , GRCh37.p13 chr1: 77,620,939-77,629,385 PIGK
    nsv6655122copy number variation1nstd229human GRCh38 chr1: 77,140,701-77,181,800 , GRCh37.p13 chr1: 77,606,386-77,647,485 PIGK
    nsv6655121copy number variation1nstd229human GRCh38 chr1: 77,136,101-77,140,700 , GRCh37.p13 chr1: 77,601,786-77,606,385 PIGK
    nsv6655120copy number variation1nstd229human GRCh38 chr1: 77,115,401-77,120,800 , GRCh37.p13 chr1: 77,581,086-77,586,485 PIGK
    nsv6655119copy number variation1nstd229human GRCh38 chr1: 77,110,818-77,116,002 , GRCh37.p13 chr1: 77,576,503-77,581,687 PIGK
    nsv6654969copy number variation1nstd229human GRCh38 chr1: 77,178,744-77,312,080 , GRCh37.p13 chr1: 77,644,429-77,777,765 AK5, LOC100421400, 2 more genes
    nsv6654882copy number variation1nstd229human GRCh38 chr1: 76,743,419-77,472,115 , GRCh37.p13 chr1: 77,209,104-77,937,800 AK5, ST6GALNAC5, 8 more genes
    nsv6654743copy number variation1nstd229human GRCh38 chr1: 77,175,593-77,181,127 , GRCh37.p13 chr1: 77,641,278-77,646,812 PIGK
    nsv6654741copy number variation1nstd229human GRCh38 chr1: 77,075,203-77,238,983 , GRCh37.p13 chr1: 77,540,888-77,704,668 PIGK, LOC100421400, 2 more genes
    nsv6654205copy number variation1nstd229human GRCh38 chr1: 77,194,161-77,194,360 , GRCh37.p13 chr1: 77,659,846-77,660,045 LOC100421400, PIGK
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