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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097022copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-138,861,289 , GRCh38.p12 chr5: 137,622,098-139,481,704 CDC25C, SLC23A1, 55 more genes
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 CDC25C, LOC100128966, 94 more genes
    nsv6797494copy number variation1nstd229human GRCh38 chr5: 138,326,474-138,329,130 , GRCh37.p13 chr5: 137,662,163-137,664,819 CDC25C
    nsv6793835copy number variation1nstd229human GRCh38 chr5: 138,039,501-138,538,500 , GRCh37.p13 chr5: 137,375,190-137,874,189 RNU6-460P, RNU6-1148P, 17 more genes
    nsv6792016copy number variation1nstd229human GRCh38 chr5: 138,323,663-138,332,139 , GRCh37.p13 chr5: 137,659,352-137,667,828 CDC25C, LOC100128966
    nsv6786278copy number variation1nstd229human GRCh38 chr5: 138,321,488-138,332,646 , GRCh37.p13 chr5: 137,657,177-137,668,335 CDC25C, LOC100128966
    nsv6782931copy number variation1nstd229human GRCh38 chr5: 138,287,737-138,295,783 , GRCh37.p13 chr5: 137,623,426-137,631,472 CDC25C
    nsv6574610inversion1nstd223human GRCh38 chr5: 138,321,725-138,322,495 , GRCh37.p13 chr5: 137,657,414-137,658,184 CDC25C
    nsv6573153inversion1nstd223human GRCh38 chr5: 138,288,198-138,288,452 , GRCh37.p13 chr5: 137,623,887-137,624,141 CDC25C
    nsv6568188inversion1nstd223human GRCh38 chr5: 138,309,511-138,309,998 , GRCh37.p13 chr5: 137,645,200-137,645,687 CDC25C
    nsv6566314inversion1nstd223human GRCh38 chr5: 138,313,201-138,313,658 , GRCh37.p13 chr5: 137,648,890-137,649,347 CDC25C
    nsv6564658inversion1nstd223human GRCh38 chr5: 138,301,889-138,302,506 , GRCh37.p13 chr5: 137,637,578-137,638,195 CDC25C
    nsv6561085inversion1nstd223human GRCh38 chr5: 138,301,966-138,302,815 , GRCh37.p13 chr5: 137,637,655-137,638,504 CDC25C
    nsv6410006copy number variation1nstd223human GRCh38 chr5: 138,321,487-138,332,645 , GRCh37.p13 chr5: 137,657,176-137,668,334 CDC25C, LOC100128966
    nsv6405600copy number variation1nstd223human GRCh38 chr5: 137,606,101-142,582,700 , GRCh37.p13 chr5: 136,941,790-141,962,265 TMCO6, PCDHB17P, 191 more genes
    nsv6401902copy number variation1nstd223human GRCh38 chr5: 138,278,473-138,288,418 , GRCh37.p13 chr5: 137,614,162-137,624,107 CDC25C
    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
    nsv6293802mobile element insertion1nstd186human GRCh37 chr5: 137,661,252-137,661,303 , GRCh38.p12 chr5: 138,325,563-138,325,614 CDC25C
    nsv6135383copy number variation1nstd213human GRCh37 chr5: 137,050,000-138,100,001 , GRCh38.p12 chr5: 137,714,311-138,764,312 CDC25C, CTNNA1, 32 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
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