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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137191copy number variation1nstd102humanPathogenic GRCh37 chr1: 1,957,148-6,553,454 , GRCh38.p12 chr1: 2,025,709-6,493,394 LOC102724429, TNFRSF14, 86 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7052066inversion1nstd229human GRCh38 chr1: 4,379,650-7,782,927 , GRCh37.p13 chr1: 4,439,710-7,842,987 NPHP4, MIR4252, 46 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv6653150copy number variation1nstd229human GRCh38 chr1: 6,334,166-6,336,535 , GRCh37.p13 chr1: 6,394,226-6,396,595 ACOT7
    nsv6653140copy number variation1nstd229human GRCh38 chr1: 6,308,723-6,314,917 , GRCh37.p13 chr1: 6,368,783-6,374,977 ACOT7
    nsv6653061copy number variation1nstd229human GRCh38 chr1: 6,381,553-6,388,030 , GRCh37.p13 chr1: 6,441,613-6,448,090 ACOT7
    nsv6653044copy number variation1nstd229human GRCh38 chr1: 6,305,222-6,309,283 , GRCh37.p13 chr1: 6,365,282-6,369,343 ACOT7
    nsv6653040copy number variation1nstd229human GRCh38 chr1: 6,302,183-6,307,561 , GRCh37.p13 chr1: 6,362,243-6,367,621 ACOT7
    nsv6653032copy number variation1nstd229human GRCh38 chr1: 6,281,309-6,281,344 , GRCh37.p13 chr1: 6,341,369-6,341,404 ACOT7
    nsv6652931copy number variation1nstd229human GRCh38 chr1: 6,377,601-6,386,900 , GRCh37.p13 chr1: 6,437,661-6,446,960 ACOT7
    nsv6652928copy number variation1nstd229human GRCh38 chr1: 6,372,248-6,374,822 , GRCh37.p13 chr1: 6,432,308-6,434,882 ACOT7
    nsv6652799copy number variation1nstd229human GRCh38 chr1: 6,269,384-6,275,974 , GRCh37.p13 chr1: 6,329,444-6,336,034 ACOT7
    nsv6652403copy number variation1nstd229human GRCh38 chr1: 6,379,101-6,385,800 , GRCh37.p13 chr1: 6,439,161-6,445,860 ACOT7
    nsv6652401copy number variation1nstd229human GRCh38 chr1: 6,378,101-6,385,800 , GRCh37.p13 chr1: 6,438,161-6,445,860 ACOT7
    nsv6652399copy number variation1nstd229human GRCh38 chr1: 6,377,101-6,385,800 , GRCh37.p13 chr1: 6,437,161-6,445,860 ACOT7
    nsv6652398copy number variation1nstd229human GRCh38 chr1: 6,377,001-6,385,900 , GRCh37.p13 chr1: 6,437,061-6,445,960 ACOT7
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