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Items: 1 to 20 of 514

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055831inversion1nstd229human GRCh38 chr5: 119,343,695-119,343,858 , GRCh37.p13 chr5: 118,679,390-118,679,553 TNFAIP8, LOC102723444
    nsv7048200inversion1nstd229human GRCh38 chr5: 119,325,162-119,334,862 , GRCh37.p13 chr5: 118,660,857-118,670,557 TNFAIP8
    nsv6774502copy number variation1nstd229human GRCh38 chr5: 119,360,736-119,360,936 , GRCh37.p13 chr5: 118,696,431-118,696,631 TNFAIP8
    nsv6774364copy number variation1nstd229human GRCh38 chr5: 119,379,308-119,383,753 , GRCh37.p13 chr5: 118,715,003-118,719,448 TNFAIP8
    nsv6769351copy number variation1nstd229human GRCh38 chr5: 119,315,064-119,317,838 , GRCh37.p13 chr5: 118,650,759-118,653,533 TNFAIP8
    nsv6768680copy number variation1nstd229human GRCh38 chr5: 119,356,358-119,367,330 , GRCh37.p13 chr5: 118,692,053-118,703,025 TNFAIP8
    nsv6768421copy number variation1nstd229human GRCh38 chr5: 119,367,887-119,445,990 , GRCh37.p13 chr5: 118,703,582-118,781,685 TNFAIP8, RNA5SP190
    nsv6768023copy number variation1nstd229human GRCh38 chr5: 119,356,145-119,367,328 , GRCh37.p13 chr5: 118,691,840-118,703,023 LOC102723444, TNFAIP8
    nsv6767794copy number variation1nstd229human GRCh38 chr5: 119,325,152-119,329,709 , GRCh37.p13 chr5: 118,660,847-118,665,404 TNFAIP8
    nsv6767610copy number variation1nstd229human GRCh38 chr5: 119,367,153-119,370,887 , GRCh37.p13 chr5: 118,702,848-118,706,582 TNFAIP8
    nsv6765120copy number variation1nstd229human GRCh38 chr5: 119,284,665-119,307,734 , GRCh37.p13 chr5: 118,620,360-118,643,429 RN7SL174P, TNFAIP8
    nsv6764811copy number variation1nstd229human GRCh38 chr5: 119,290,156-119,290,189 , GRCh37.p13 chr5: 118,625,851-118,625,884 TNFAIP8
    nsv6764469copy number variation1nstd229human GRCh38 chr5: 118,517,046-119,389,840 , GRCh37.p13 chr5: 117,852,741-118,725,535 LINC02208, MIR5706, 16 more genes
    nsv6763622copy number variation1nstd229human GRCh38 chr5: 119,388,816-119,392,411 , GRCh37.p13 chr5: 118,724,511-118,728,106 TNFAIP8
    nsv6763310copy number variation1nstd229human GRCh38 chr5: 119,287,034-119,300,039 , GRCh37.p13 chr5: 118,622,729-118,635,734 TNFAIP8
    nsv6760846copy number variation1nstd229human GRCh38 chr5: 119,388,649-119,602,902 , GRCh37.p13 chr5: 118,724,344-118,938,597 TNFAIP8, RPL21P58, 4 more genes
    nsv6760254copy number variation1nstd229human GRCh38 chr5: 119,383,740-119,383,882 , GRCh37.p13 chr5: 118,719,435-118,719,577 TNFAIP8
    nsv6759479copy number variation1nstd229human GRCh38 chr5: 119,345,086-119,349,396 , GRCh37.p13 chr5: 118,680,781-118,685,091 TNFAIP8, LOC102723444
    nsv6758684copy number variation1nstd229human GRCh38 chr5: 119,341,959-119,341,994 , GRCh37.p13 chr5: 118,677,654-118,677,689 TNFAIP8
    nsv6637111copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606 SLC12A2, CCDC192, 180 more genes
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