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Items: 1 to 20 of 316

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7146497insertion1nstd232human GRCh37.p13 chr5: 10,288,641-10,288,641 , GRCh38.p12 chr5: 10,288,529-10,288,529 CMBL
    nsv7098841copy number variation1nstd102humanPathogenic GRCh37 chr5: 10,149,255-18,180,300 , GRCh38.p12 chr5: 10,149,143-18,180,191 RN7SKP133, TAF11L1, 102 more genes
    nsv7052860inversion1nstd229human GRCh38 chr5: 10,170,489-10,504,221 , GRCh37.p13 chr5: 10,170,601-10,504,333 CMBL, MIR10397, 11 more genes
    nsv7046143inversion1nstd229human GRCh38 chr5: 10,272,945-10,347,455 , GRCh37.p13 chr5: 10,273,057-10,347,567 LOC105374651, CMBL, 1 more genes
    nsv7045933inversion1nstd229human GRCh38 chr5: 9,205,469-10,383,964 , GRCh37.p13 chr5: 9,205,581-10,384,076 SEMA5A-AS1, SNORD123, 15 more genes
    nsv6777926copy number variation1nstd229human GRCh38 chr5: 10,299,289-10,313,565 , GRCh37.p13 chr5: 10,299,401-10,313,677 CMBL
    nsv6775933copy number variation1nstd229human GRCh38 chr5: 10,282,665-10,292,707 , GRCh37.p13 chr5: 10,282,777-10,292,819 CMBL
    nsv6772926copy number variation1nstd229human GRCh38 chr5: 10,294,747-10,298,565 , GRCh37.p13 chr5: 10,294,859-10,298,677 CMBL
    nsv6768738copy number variation1nstd229human GRCh38 chr5: 10,299,600-10,304,715 , GRCh37.p13 chr5: 10,299,712-10,304,827 CMBL
    nsv6767593copy number variation1nstd229human GRCh38 chr5: 10,283,512-10,286,288 , GRCh37.p13 chr5: 10,283,624-10,286,400 CMBL
    nsv6766002copy number variation1nstd229human GRCh38 chr5: 10,203,601-10,797,600 , GRCh37.p13 chr5: 10,203,713-10,797,712 LOC645763, DAP, 16 more genes
    nsv6765511copy number variation1nstd229human GRCh38 chr5: 10,137,393-10,304,241 , GRCh37.p13 chr5: 10,137,505-10,304,353 CMBL, ATPSCKMT, 1 more genes
    nsv6764486copy number variation1nstd229human GRCh38 chr5: 9,477,059-10,373,440 , GRCh37.p13 chr5: 9,477,171-10,373,552 LOC107986405, MARCHF6-DT, 15 more genes
    nsv6762136copy number variation1nstd229human GRCh38 chr5: 10,298,018-10,301,817 , GRCh37.p13 chr5: 10,298,130-10,301,929 CMBL
    nsv6760101copy number variation1nstd229human GRCh38 chr5: 10,278,009-10,284,872 , GRCh37.p13 chr5: 10,278,121-10,284,984 CMBL
    nsv6758544copy number variation1nstd229human GRCh38 chr5: 10,286,016-10,288,124 , GRCh37.p13 chr5: 10,286,128-10,288,236 CMBL
    nsv6637149copy number variation1nstd102humanPathogenic GRCh37 chr5: 8,081,005-22,210,970 , GRCh38.p12 chr5: 8,080,892-22,210,861 LOC107986376, MARCHF11, 150 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636849copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678 ADCY2, HMGB3P3, 248 more genes
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