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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097518copy number variation1nstd102humanUncertain significance GRCh37 chr5: 150,704,827-150,705,033 , GRCh38.p12 chr5: 151,325,266-151,325,472 SLC36A2
    nsv7097517copy number variation1nstd102humanUncertain significance GRCh37 chr5: 150,632,778-150,727,021 , GRCh38.p12 chr5: 151,253,217-151,347,460 ATP6V1G1P5, SLC36A3, 2 more genes
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv6796388copy number variation1nstd229human GRCh38 chr5: 151,321,827-151,580,900 , GRCh37.p13 chr5: 150,701,388-150,960,461 RNA5SP197, LOC100419720, 6 more genes
    nsv6793207copy number variation1nstd229human GRCh38 chr5: 151,320,312-151,323,636 , GRCh37.p13 chr5: 150,699,873-150,703,197 SLC36A2
    nsv6793049copy number variation1nstd229human GRCh38 chr5: 151,340,640-151,346,383 , GRCh37.p13 chr5: 150,720,201-150,725,944 SLC36A2
    nsv6792675copy number variation1nstd229human GRCh38 chr5: 151,329,765-151,342,992 , GRCh37.p13 chr5: 150,709,326-150,722,553 SLC36A2
    nsv6789981copy number variation1nstd229human GRCh38 chr5: 151,317,108-151,319,705 , GRCh37.p13 chr5: 150,696,669-150,699,266 ATP6V1G1P5, SLC36A2
    nsv6787484copy number variation1nstd229human GRCh38 chr5: 151,330,497-151,334,792 , GRCh37.p13 chr5: 150,710,058-150,714,353 SLC36A2
    nsv6787407copy number variation1nstd229human GRCh38 chr5: 151,310,997-151,318,986 , GRCh37.p13 chr5: 150,690,558-150,698,547 ATP6V1G1P5, SLC36A2
    nsv6784928copy number variation1nstd229human GRCh38 chr5: 151,326,033-151,330,107 , GRCh37.p13 chr5: 150,705,594-150,709,668 SLC36A2
    nsv6783993copy number variation1nstd229human GRCh38 chr5: 151,331,476-151,337,382 , GRCh37.p13 chr5: 150,711,037-150,716,943 SLC36A2
    nsv6779590copy number variation1nstd229human GRCh38 chr5: 151,324,438-151,332,012 , GRCh37.p13 chr5: 150,703,999-150,711,573 SLC36A2
    nsv6778149copy number variation1nstd229human GRCh38 chr5: 151,245,914-151,331,227 , GRCh37.p13 chr5: 150,625,475-150,710,788 SLC36A3, SLC36A2, 2 more genes
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6636466copy number variation1nstd102humanUncertain significance GRCh37 chr5: 150,706,776-150,954,695 , GRCh38.p12 chr5: 151,327,215-151,575,134 LOC105378234, LOC100419720, 6 more genes
    nsv6556254inversion1nstd223human GRCh38 chr5: 151,316,933-151,317,806 , GRCh37.p13 chr5: 150,696,494-150,697,367 ATP6V1G1P5, SLC36A2
    nsv6411072copy number variation1nstd223human GRCh38 chr5: 151,330,497-151,334,787 , GRCh37.p13 chr5: 150,710,058-150,714,348 SLC36A2
    nsv6403642copy number variation1nstd223human GRCh38 chr5: 151,327,556-151,328,195 , GRCh37.p13 chr5: 150,707,117-150,707,756 SLC36A2
    nsv6400892copy number variation1nstd223human GRCh38 chr5: 151,324,431-151,332,010 , GRCh37.p13 chr5: 150,703,992-150,711,571 SLC36A2
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