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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7042796inversion1nstd229human GRCh38 chr5: 134,802,336-135,650,849 , GRCh37.p13 chr5: 134,138,026-134,986,538 TXNDC15, LINC02900, 20 more genes
    nsv6790036copy number variation1nstd229human GRCh38 chr5: 135,452,102-135,455,154 , GRCh37.p13 chr5: 134,787,792-134,790,844 TIFAB
    nsv6787056copy number variation1nstd229human GRCh38 chr5: 126,804,198-136,494,917 , GRCh37.p13 chr5: 126,139,890-135,830,606 SLC22A4, LOC105379199, 158 more genes
    nsv6780184copy number variation1nstd229human GRCh38 chr5: 135,449,944-135,450,111 , GRCh37.p13 chr5: 134,785,634-134,785,801 TIFAB
    nsv6636280copy number variation1nstd102humanUncertain significance GRCh37 chr5: 134,524,754-135,283,222 , GRCh38.p12 chr5: 135,189,064-135,947,533 LINC02900, DCANP1, 12 more genes
    nsv6406778copy number variation1nstd223human GRCh38 chr5: 135,449,809-135,451,625 , GRCh37.p13 chr5: 134,785,499-134,787,315 TIFAB
    nsv6398663copy number variation1nstd223human GRCh38 chr5: 135,437,966-135,447,739 , GRCh37.p13 chr5: 134,773,656-134,783,429 TIFAB, DCANP1
    nsv6313595copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,031,902-137,623,639 , GRCh38.p12 chr5: 132,696,210-138,287,950 TGFBI, RPS10P11, 110 more genes
    nsv6313506copy number variation1nstd102humanUncertain significance GRCh37 chr5: 132,829,317-134,983,855 , GRCh38.p12 chr5: 133,493,625-135,648,166 RPS10P11, PCBD2, 47 more genes
    nsv6135646copy number variation1nstd213human GRCh37 chr5: 124,370,000-136,400,001 , GRCh38.p12 chr5: 125,034,307-137,064,312 ACTBP4, ALDH7A1, 181 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135114copy number variation1nstd213human GRCh37 chr5: 133,550,000-135,990,001 , GRCh38.p12 chr5: 134,214,309-136,654,312 CAMLG, IL9, 53 more genes
    nsv6003365copy number variation1nstd212human GRCh38 chr5: 135,452,392-135,452,454 , GRCh37.p13 chr5: 134,788,082-134,788,144 TIFAB
    nsv5454726copy number variation1nstd206human GRCh38 chr5: 135,445,854-135,447,661 , GRCh37.p13 chr5: 134,781,544-134,783,351 TIFAB, DCANP1
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4938716copy number variation1nstd200human GRCh38 chr5: 135,449,808-135,451,626 , GRCh37.p13 chr5: 134,785,498-134,787,316 TIFAB
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4658970copy number variation1nstd186human GRCh37 chr5: 134,781,542-134,783,351 , GRCh38.p12 chr5: 135,445,852-135,447,661 TIFAB, DCANP1
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