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Items: 1 to 20 of 269

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7093811copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,974,585-91,222,335 , GRCh38.p12 chr10: 89,214,828-89,462,578 SLC16A12-AS1, IFIT1, 10 more genes
    nsv7074617inversion1nstd229human GRCh38 chr10: 86,025,751-89,446,782 , GRCh37.p13 chr10: 87,785,508-91,206,539 GRID1, LDB3, 83 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7066369inversion1nstd229human GRCh38 chr10: 89,442,757-89,442,880 , GRCh37.p13 chr10: 91,202,514-91,202,637 SLC16A12
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6897508copy number variation1nstd229human GRCh38 chr10: 89,499,201-89,505,100 , GRCh37.p13 chr10: 91,258,958-91,264,857 SLC16A12
    nsv6896619copy number variation1nstd229human GRCh38 chr10: 89,465,685-89,471,148 , GRCh37.p13 chr10: 91,225,442-91,230,905 SLC16A12, SLC16A12-AS1
    nsv6895729copy number variation1nstd229human GRCh38 chr10: 89,502,548-89,608,022 , GRCh37.p13 chr10: 91,262,305-91,367,779 MIR107, PANK1, 1 more genes
    nsv6894040copy number variation1nstd229human GRCh38 chr10: 89,494,510-89,500,744 , GRCh37.p13 chr10: 91,254,267-91,260,501 SLC16A12
    nsv6893399copy number variation1nstd229human GRCh38 chr10: 89,534,581-89,535,770 , GRCh37.p13 chr10: 91,294,338-91,295,527 SLC16A12
    nsv6892850copy number variation1nstd229human GRCh38 chr10: 89,536,390-89,545,791 , GRCh37.p13 chr10: 91,296,147-91,305,548 SLC16A12
    nsv6890324copy number variation1nstd229human GRCh38 chr10: 89,524,315-89,531,252 , GRCh37.p13 chr10: 91,284,072-91,291,009 SLC16A12
    nsv6887780copy number variation1nstd229human GRCh38 chr10: 89,504,472-89,512,821 , GRCh37.p13 chr10: 91,264,229-91,272,578 SLC16A12
    nsv6887742copy number variation1nstd229human GRCh38 chr10: 89,432,301-89,438,900 , GRCh37.p13 chr10: 91,192,058-91,198,657 SLC16A12
    nsv6887645copy number variation1nstd229human GRCh38 chr10: 89,425,851-89,428,531 , GRCh37.p13 chr10: 91,185,608-91,188,288 SLC16A12
    nsv6886896copy number variation1nstd229human GRCh38 chr10: 89,451,954-89,466,810 , GRCh37.p13 chr10: 91,211,711-91,226,567 SLC16A12, SLC16A12-AS1
    nsv6886587copy number variation1nstd229human GRCh38 chr10: 89,381,823-89,442,318 , GRCh37.p13 chr10: 91,141,580-91,202,075 LOC107984251, IFIT1B, 3 more genes
    nsv6884235copy number variation1nstd229human GRCh38 chr10: 89,451,476-89,457,418 , GRCh37.p13 chr10: 91,211,233-91,217,175 SLC16A12-AS1, SLC16A12
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