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Items: 1 to 20 of 961

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148086copy number variation1nstd102humanPathogenic GRCh37 chr10: 124,895,517-135,440,296 , GRCh38.p12 chr10: 123,136,001-133,626,792 FANK1, LOC105378534, 159 more genes
    nsv7145327insertion1nstd232human GRCh37.p13 chr10: 134,436,399-134,436,399 , GRCh38.p12 chr10: 132,622,895-132,622,895 INPP5A
    nsv7143465copy number variation1nstd232human GRCh37.p13 chr10: 134,585,204-134,585,257 , GRCh38.p12 chr10: 132,771,700-132,771,753 INPP5A
    nsv7143323insertion1nstd232human GRCh37.p13 chr10: 134,581,316-134,581,316 , GRCh38.p12 chr10: 132,767,812-132,767,812 INPP5A
    nsv7141658copy number variation1nstd232human GRCh37.p13 chr10: 134,555,227-134,555,281 , GRCh38.p12 chr10: 132,741,723-132,741,777 INPP5A
    nsv7139219copy number variation1nstd232human GRCh37.p13 chr10: 134,585,162-134,585,215 , GRCh38.p12 chr10: 132,771,658-132,771,711 INPP5A
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7137208copy number variation1nstd102humanPathogenic GRCh37 chr10: 123,477,898-135,427,143 , GRCh38.p12 chr10: 121,718,384-133,613,639 ZRANB1, LOC105378544, 182 more genes
    nsv7098893copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306 LOC105378571, DOCK1, 196 more genes
    nsv7075546inversion1nstd229human GRCh38 chr10: 132,775,990-133,166,126 , GRCh37.p13 chr10: 134,589,494-134,979,630 LOC105378571, LINC01167, 12 more genes
    nsv7072362inversion1nstd229human GRCh38 chr10: 132,563,693-132,563,734 , GRCh37.p13 chr10: 134,377,197-134,377,238 INPP5A
    nsv7067407inversion1nstd229human GRCh38 chr10: 132,648,726-132,648,822 , GRCh37.p13 chr10: 134,462,230-134,462,326 INPP5A
    nsv7062432inversion1nstd229human GRCh38 chr10: 132,713,158-132,713,218 , GRCh37.p13 chr10: 134,526,662-134,526,722 INPP5A
    nsv6897801copy number variation1nstd229human GRCh38 chr10: 132,704,338-132,707,476 , GRCh37.p13 chr10: 134,517,842-134,520,980 INPP5A
    nsv6896360copy number variation1nstd229human GRCh38 chr10: 132,700,401-132,778,300 , GRCh37.p13 chr10: 134,513,905-134,591,804 INPP5A
    nsv6896315copy number variation1nstd229human GRCh38 chr10: 132,651,163-132,653,015 , GRCh37.p13 chr10: 134,464,667-134,466,519 INPP5A
    nsv6895070copy number variation1nstd229human GRCh38 chr10: 132,639,934-132,640,087 , GRCh37.p13 chr10: 134,453,438-134,453,591 INPP5A
    nsv6895066copy number variation1nstd229human GRCh38 chr10: 132,717,274-132,717,683 , GRCh37.p13 chr10: 134,530,778-134,531,187 INPP5A
    nsv6894915copy number variation1nstd229human GRCh38 chr10: 132,715,387-132,715,527 , GRCh37.p13 chr10: 134,528,891-134,529,031 INPP5A
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