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Items: 1 to 20 of 231

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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
    nsv7053972inversion1nstd229human GRCh38 chr5: 136,476,162-137,977,595 , GRCh37.p13 chr5: 135,811,851-137,313,284 FAM13B, SPOCK1, 12 more genes
    nsv7042674inversion1nstd229human GRCh38 chr5: 137,921,764-137,921,807 , GRCh37.p13 chr5: 137,257,453-137,257,496 PKD2L2
    nsv6793945copy number variation1nstd229human GRCh38 chr5: 137,892,807-137,898,208 , GRCh37.p13 chr5: 137,228,496-137,233,897 PKD2L2
    nsv6787367copy number variation1nstd229human GRCh38 chr5: 137,886,901-137,896,100 , GRCh37.p13 chr5: 137,222,590-137,231,789 MYOT, PKD2L2-DT, 1 more genes
    nsv6786392copy number variation1nstd229human GRCh38 chr5: 137,919,401-137,923,500 , GRCh37.p13 chr5: 137,255,090-137,259,189 PKD2L2
    nsv6778243copy number variation1nstd229human GRCh38 chr5: 137,914,684-137,919,826 , GRCh37.p13 chr5: 137,250,373-137,255,515 PKD2L2
    nsv6571796inversion1nstd223human GRCh38 chr5: 137,922,576-137,922,693 , GRCh37.p13 chr5: 137,258,265-137,258,382 PKD2L2
    nsv6561573inversion1nstd223human GRCh38 chr5: 137,922,583-137,923,018 , GRCh37.p13 chr5: 137,258,272-137,258,707 PKD2L2
    nsv6559925inversion1nstd223human GRCh38 chr5: 137,920,732-137,923,184 , GRCh37.p13 chr5: 137,256,421-137,258,873 PKD2L2
    nsv6414500copy number variation1nstd223human GRCh38 chr5: 137,926,552-137,927,030 , GRCh37.p13 chr5: 137,262,241-137,262,719 PKD2L2
    nsv6408812copy number variation1nstd223human GRCh38 chr5: 137,909,757-137,911,916 , GRCh37.p13 chr5: 137,245,446-137,247,605 PKD2L2
    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
    nsv6403485copy number variation1nstd223human GRCh38 chr5: 137,914,337-137,965,735 , GRCh37.p13 chr5: 137,250,026-137,301,424 PKD2L2, FAM13B
    nsv6401851copy number variation1nstd223human GRCh38 chr5: 137,937,001-137,938,884 , GRCh37.p13 chr5: 137,272,690-137,274,573 PKD2L2, FAM13B
    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
    nsv6135384copy number variation1nstd213human GRCh37 chr5: 137,160,000-137,330,001 , GRCh38.p12 chr5: 137,824,311-137,994,312 MYOT, PKD2L2, 3 more genes
    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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