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Items: 1 to 20 of 615

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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
    nsv7055498inversion1nstd229human GRCh38 chr1: 66,514,766-73,182,042 , GRCh37.p13 chr1: 66,980,449-73,647,725 LINC02796, LOC105378789, 80 more genes
    nsv7054185inversion1nstd229human GRCh38 chr1: 70,944,942-71,304,316 , GRCh37.p13 chr1: 71,410,625-71,769,999 PTGER3, ZRANB2, 4 more genes
    nsv7053920inversion1nstd229human GRCh38 chr1: 67,470,120-71,187,985 , GRCh37.p13 chr1: 67,935,803-71,653,668 LOC107984967, LOC105378787, 53 more genes
    nsv7051964inversion1nstd229human GRCh38 chr1: 67,266,655-71,123,545 , GRCh37.p13 chr1: 67,732,338-71,589,228 CHORDC1P5, IL12RB2, 58 more genes
    nsv7046421inversion1nstd229human GRCh38 chr1: 70,944,938-71,316,191 , GRCh37.p13 chr1: 71,410,621-71,781,874 ZRANB2-AS1, ZRANB2-DT, 4 more genes
    nsv6654043copy number variation1nstd229human GRCh38 chr1: 71,021,497-71,024,096 , GRCh37.p13 chr1: 71,487,180-71,489,779 PTGER3
    nsv6654042copy number variation1nstd229human GRCh38 chr1: 71,021,232-71,024,071 , GRCh37.p13 chr1: 71,486,915-71,489,754 PTGER3
    nsv6654041copy number variation1nstd229human GRCh38 chr1: 70,985,561-70,988,328 , GRCh37.p13 chr1: 71,451,244-71,454,011 PTGER3
    nsv6654040copy number variation1nstd229human GRCh38 chr1: 70,964,001-71,006,100 , GRCh37.p13 chr1: 71,429,684-71,471,783 PTGER3
    nsv6654039copy number variation1nstd229human GRCh38 chr1: 70,949,101-71,001,300 , GRCh37.p13 chr1: 71,414,784-71,466,983 PTGER3
    nsv6654038copy number variation1nstd229human GRCh38 chr1: 70,942,401-71,012,600 , GRCh37.p13 chr1: 71,408,084-71,478,283 PTGER3
    nsv6654037copy number variation1nstd229human GRCh38 chr1: 70,926,702-70,927,283 , GRCh37.p13 chr1: 71,392,385-71,392,966 PTGER3
    nsv6654036copy number variation1nstd229human GRCh38 chr1: 70,901,184-70,992,217 , GRCh37.p13 chr1: 71,366,867-71,457,900 PTGER3
    nsv6654025copy number variation1nstd229human GRCh38 chr1: 70,670,691-70,963,513 , GRCh37.p13 chr1: 71,136,374-71,429,196 LINC01788, LOC102724572, 1 more genes
    nsv6653978copy number variation1nstd229human GRCh38 chr1: 71,021,324-71,024,089 , GRCh37.p13 chr1: 71,487,007-71,489,772 PTGER3
    nsv6653977copy number variation1nstd229human GRCh38 chr1: 71,017,195-71,019,264 , GRCh37.p13 chr1: 71,482,878-71,484,947 PTGER3
    nsv6653976copy number variation1nstd229human GRCh38 chr1: 70,979,901-70,984,400 , GRCh37.p13 chr1: 71,445,584-71,450,083 PTGER3
    nsv6653975copy number variation1nstd229human GRCh38 chr1: 70,969,191-70,986,332 , GRCh37.p13 chr1: 71,434,874-71,452,015 PTGER3
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