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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048173inversion1nstd229human GRCh38 chr3: 165,654,396-165,958,369 , GRCh37.p13 chr3: 165,372,184-165,676,157 BCHE
    nsv7041721inversion1nstd229human GRCh38 chr3: 165,680,578-165,867,868 , GRCh37.p13 chr3: 165,398,366-165,585,656 BCHE
    nsv6736275copy number variation1nstd229human GRCh38 chr3: 165,807,201-165,809,000 , GRCh37.p13 chr3: 165,524,989-165,526,788 BCHE
    nsv6736155copy number variation1nstd229human GRCh38 chr3: 165,795,450-165,797,034 , GRCh37.p13 chr3: 165,513,238-165,514,822 BCHE
    nsv6734829copy number variation1nstd229human GRCh38 chr3: 165,799,965-165,801,189 , GRCh37.p13 chr3: 165,517,753-165,518,977 BCHE
    nsv6730982copy number variation1nstd229human GRCh38 chr3: 165,802,391-165,832,127 , GRCh37.p13 chr3: 165,520,179-165,549,915 BCHE
    nsv6730926copy number variation1nstd229human GRCh38 chr3: 165,652,757-166,817,336 , GRCh37.p13 chr3: 165,370,545-166,535,124 PSAT1P4, MCUR1P2, 7 more genes
    nsv6729920copy number variation1nstd229human GRCh38 chr3: 165,814,827-165,830,799 , GRCh37.p13 chr3: 165,532,615-165,548,587 BCHE
    nsv6729060copy number variation1nstd229human GRCh38 chr3: 165,788,701-165,793,100 , GRCh37.p13 chr3: 165,506,489-165,510,888 BCHE
    nsv6726158copy number variation1nstd229human GRCh38 chr3: 165,768,820-165,773,338 , GRCh37.p13 chr3: 165,486,608-165,491,126 BCHE
    nsv6725515copy number variation1nstd229human GRCh38 chr3: 165,782,321-165,782,436 , GRCh37.p13 chr3: 165,500,109-165,500,224 BCHE
    nsv6723988copy number variation1nstd229human GRCh38 chr3: 165,593,744-167,293,427 , GRCh37.p13 chr3: 165,311,532-167,011,215 LOC105374196, LOC105374193, 12 more genes
    nsv6723217copy number variation1nstd229human GRCh38 chr3: 165,809,603-165,809,631 , GRCh37.p13 chr3: 165,527,391-165,527,419 BCHE
    nsv6722606copy number variation1nstd229human GRCh38 chr3: 165,831,475-165,848,104 , GRCh37.p13 chr3: 165,549,263-165,565,892 BCHE
    nsv6721979copy number variation1nstd229human GRCh38 chr3: 165,796,379-165,811,100 , GRCh37.p13 chr3: 165,514,167-165,528,888 BCHE
    nsv6721736copy number variation1nstd229human GRCh38 chr3: 165,670,862-165,909,050 , GRCh37.p13 chr3: 165,388,650-165,626,838 BCHE
    nsv6721601copy number variation1nstd229human GRCh38 chr3: 165,729,997-165,943,663 , GRCh37.p13 chr3: 165,447,785-165,661,451 BCHE
    nsv6721002copy number variation1nstd229human GRCh38 chr3: 165,736,451-165,822,557 , GRCh37.p13 chr3: 165,454,239-165,540,345 BCHE
    nsv6720415copy number variation1nstd229human GRCh38 chr3: 165,788,819-165,790,615 , GRCh37.p13 chr3: 165,506,607-165,508,403 BCHE
    nsv6719264copy number variation1nstd229human GRCh38 chr3: 165,774,596-165,784,345 , GRCh37.p13 chr3: 165,492,384-165,502,133 BCHE
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