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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv6874223copy number variation1nstd229human GRCh38 chr9: 129,345,745-129,346,126 , GRCh37.p13 chr9: 132,108,024-132,108,405 LINC01503
    nsv6871996copy number variation1nstd229human GRCh38 chr9: 129,336,690-129,340,166 , GRCh37.p13 chr9: 132,098,969-132,102,445 LINC01503
    nsv6870138copy number variation1nstd229human GRCh38 chr9: 129,284,492-129,343,256 , GRCh37.p13 chr9: 132,046,771-132,105,535 LINC02913, LINC01503, 2 more genes
    nsv6869550copy number variation1nstd229human GRCh38 chr9: 129,339,757-129,342,172 , GRCh37.p13 chr9: 132,102,036-132,104,451 LINC01503
    nsv6868595copy number variation1nstd229human GRCh38 chr9: 129,339,601-129,648,300 , GRCh37.p13 chr9: 132,101,880-132,410,579 LOC105376291, C9orf50, 7 more genes
    nsv6862247copy number variation1nstd229human GRCh38 chr9: 129,340,788-129,340,862 , GRCh37.p13 chr9: 132,103,067-132,103,141 LINC01503
    nsv6442353copy number variation1nstd223human GRCh38 chr9: 129,342,701-129,344,400 , GRCh37.p13 chr9: 132,104,980-132,106,679 LINC01503
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291261copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529 PTPA, AK1, 123 more genes
    nsv6269913copy number variation1nstd214human GRCh38 chr9: 129,340,788-129,340,861 , GRCh37.p13 chr9: 132,103,067-132,103,140 LINC01503
    nsv6171560copy number variation1nstd214human GRCh38 chr9: 129,340,574-129,340,755 , GRCh37.p13 chr9: 132,102,853-132,103,034 LINC01503
    nsv6137057copy number variation1nstd213human GRCh37 chr9: 130,360,000-135,460,001 , GRCh38.p12 chr9: 127,597,721-132,584,614 CRAT, GLE1, 145 more genes
    nsv6003161copy number variation1nstd212human GRCh38 chr9: 129,340,797-129,340,873 , GRCh37.p13 chr9: 132,103,076-132,103,152 LINC01503
    nsv5926948copy number variation1nstd209human GRCh38 chr9: 129,340,788-129,340,861 , GRCh37.p13 chr9: 132,103,067-132,103,140 LINC01503
    nsv5920670copy number variation1nstd209human GRCh38 chr9: 129,340,606-129,340,861 , GRCh37.p13 chr9: 132,102,885-132,103,140 LINC01503
    nsv5317383copy number variation1nstd204human GRCh38.p13 chr9: 129,344,674-129,344,766 , GRCh37.p13 chr9: 132,106,953-132,107,045 LINC01503
    nsv4985756copy number variation1nstd200human GRCh38 chr9: 129,327,341-129,430,882 , GRCh37.p13 chr9: 132,089,620-132,193,161 RN7SL159P, LINC01503, 1 more genes
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