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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097217copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,908,818-10,085,568 , GRCh38.p12 chr3: 9,867,134-10,043,884 EMC3, PRRT3, 14 more genes
    nsv7055847inversion1nstd229human GRCh38 chr3: 5,111,802-11,290,661 , GRCh37.p13 chr3: 5,153,487-11,332,347 GHRLOS, LHFPL4, 96 more genes
    nsv7054108inversion1nstd229human GRCh38 chr3: 9,870,357-10,024,166 , GRCh37.p13 chr3: 9,912,041-10,065,850 PRRT3-AS1, CRELD1, 12 more genes
    nsv7042755inversion1nstd229human GRCh38 chr3: 8,982,205-12,221,239 , GRCh37.p13 chr3: 9,023,889-12,262,739 SYN2, MTCO1P5, 74 more genes
    nsv6717492copy number variation1nstd229human GRCh38 chr3: 9,728,301-10,020,500 , GRCh37.p13 chr3: 9,769,985-10,062,184 CPNE9, OGG1, 22 more genes
    nsv6715869copy number variation1nstd229human GRCh38 chr3: 9,686,801-10,627,600 , GRCh37.p13 chr3: 9,728,485-10,669,285 FANCD2OS, CRELD1, 40 more genes
    nsv6708321copy number variation1nstd229human GRCh38 chr3: 9,926,501-9,958,600 , GRCh37.p13 chr3: 9,968,185-10,000,284 PRRT3-AS1, IL17RC, 2 more genes
    nsv6704578copy number variation1nstd229human GRCh38 chr3: 9,886,882-9,933,807 , GRCh37.p13 chr3: 9,928,566-9,975,491 RNU6-882P, JAGN1, 3 more genes
    nsv6704243copy number variation1nstd229human GRCh38 chr3: 9,926,979-9,935,804 , GRCh37.p13 chr3: 9,968,663-9,977,488 IL17RC, CRELD1
    nsv6701779copy number variation1nstd229human GRCh38 chr3: 9,923,511-9,929,275 , GRCh37.p13 chr3: 9,965,195-9,970,959 IL17RC
    nsv6637145copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,931-10,687,964 , GRCh38.p12 chr3: 19,253-10,646,279 RN7SL120P, LOC105376940, 132 more genes
    nsv6636952copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,908,803-10,265,564 , GRCh38.p12 chr3: 9,867,119-10,223,880 CIDECP1, CIDEC, 19 more genes
    nsv6636289copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,754,612-10,295,828 , GRCh38.p12 chr3: 9,712,928-10,254,144 FANCD2P1, RNU6-882P, 30 more genes
    nsv6636276copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035 RPL23AP39, LOC107986059, 144 more genes
    nsv6545393inversion1nstd223human GRCh38 chr3: 9,926,270-9,927,315 , GRCh37.p13 chr3: 9,967,954-9,968,999 IL17RC
    nsv6541643inversion1nstd223human GRCh38 chr3: 9,921,790-9,923,106 , GRCh37.p13 chr3: 9,963,474-9,964,790 IL17RC
    nsv6540919inversion1nstd223human GRCh38 chr3: 9,115,607-13,898,149 , GRCh37.p13 chr3: 9,157,291-13,939,646 MKRN2OS, RAF1, 106 more genes
    nsv6366552copy number variation1nstd223human GRCh38 chr3: 9,857,297-10,031,325 , GRCh37.p13 chr3: 9,898,981-10,073,009 PRRT3-AS1, IL17RE, 13 more genes
    nsv6358983copy number variation1nstd223human GRCh38 chr3: 9,923,511-9,929,275 , GRCh37.p13 chr3: 9,965,195-9,970,959 IL17RC
    nsv6358519copy number variation1nstd223human GRCh38 chr3: 9,922,563-9,926,323 , GRCh37.p13 chr3: 9,964,247-9,968,007 IL17RC
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