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Items: 1 to 20 of 241

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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
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 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
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6889723copy number variation1nstd229human GRCh38 chr10: 91,810,940-91,811,568 , GRCh37.p13 chr10: 93,570,697-93,571,325 TNKS2
    nsv6889274copy number variation1nstd229human GRCh38 chr10: 91,846,715-91,846,747 , GRCh37.p13 chr10: 93,606,472-93,606,504 TNKS2
    nsv6886593copy number variation1nstd229human GRCh38 chr10: 91,845,697-91,852,724 , GRCh37.p13 chr10: 93,605,454-93,612,481 TNKS2
    nsv6885557copy number variation1nstd229human GRCh38 chr10: 91,862,091-91,883,491 , GRCh37.p13 chr10: 93,621,848-93,643,248 TNKS2
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637584copy number variation1nstd102humanUncertain significance GRCh37 chr10: 93,577,943-93,922,822 , GRCh38.p12 chr10: 91,818,186-92,163,065 EIF4A1P8, CPEB3, 5 more genes
    nsv6620929copy number variation1nstd224human GRCh37 chr10: 93,412,994-94,014,958 , GRCh38.p12 chr10: 91,653,237-92,255,201 EIF4A1P8, LOC107984253, 11 more genes
    nsv6594667inversion1nstd223human GRCh38 chr10: 91,838,902-91,840,313 , GRCh37.p13 chr10: 93,598,659-93,600,070 TNKS2
    nsv6585251inversion1nstd223human GRCh38 chr10: 91,822,596-91,822,929 , GRCh37.p13 chr10: 93,582,353-93,582,686 TNKS2
    nsv6580534inversion1nstd223human GRCh38 chr10: 91,810,345-91,810,529 , GRCh37.p13 chr10: 93,570,102-93,570,286 TNKS2
    nsv6576964inversion1nstd223human GRCh38 chr10: 91,848,845-91,850,371 , GRCh37.p13 chr10: 93,608,602-93,610,128 TNKS2
    nsv6452429copy number variation1nstd223human GRCh38 chr10: 91,823,397-91,825,168 , GRCh37.p13 chr10: 93,583,154-93,584,925 TNKS2
    nsv6451053copy number variation1nstd223human GRCh38 chr10: 91,859,426-91,860,147 , GRCh37.p13 chr10: 93,619,183-93,619,904 TNKS2
    nsv6446818copy number variation1nstd223human GRCh38 chr10: 91,863,883-91,864,241 , GRCh37.p13 chr10: 93,623,640-93,623,998 TNKS2
    nsv6445575copy number variation1nstd223human GRCh38 chr10: 91,861,123-91,861,607 , GRCh37.p13 chr10: 93,620,880-93,621,364 TNKS2
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