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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148081copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,167,260-12,533,766 , GRCh38.p12 chr3: 10,125,576-12,492,267 SLC6A1-AS1, LOC101927467, 37 more genes
    nsv7144987insertion1nstd232human GRCh37.p13 chr3: 10,353,785-10,353,785 , GRCh38.p12 chr3: 10,312,101-10,312,101 SEC13
    nsv7096528copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,094,051-11,078,652 , GRCh38.p12 chr3: 10,052,367-11,036,966 LINC00606, MIR378B, 19 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
    nsv7042755inversion1nstd229human GRCh38 chr3: 8,982,205-12,221,239 , GRCh37.p13 chr3: 9,023,889-12,262,739 SYN2, MTCO1P5, 74 more genes
    nsv7041321inversion1nstd229human GRCh38 chr3: 10,273,886-10,365,534 , GRCh37.p13 chr3: 10,315,570-10,407,218 TATDN2, ATP2B2, 6 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
    nsv6705227copy number variation1nstd229human GRCh38 chr3: 10,301,720-10,301,853 , GRCh37.p13 chr3: 10,343,404-10,343,537 SEC13
    nsv6698744copy number variation1nstd229human GRCh38 chr3: 10,083,301-10,510,500 , GRCh37.p13 chr3: 10,124,985-10,552,184 MIR885, IRAK2, 12 more genes
    nsv6637145copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,931-10,687,964 , GRCh38.p12 chr3: 19,253-10,646,279 RN7SL120P, LOC105376940, 132 more genes
    nsv6637039copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,024,917-11,917,048 , GRCh38.p12 chr3: 9,983,233-11,875,574 ATG7, GHRL, 35 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
    nsv6540919inversion1nstd223human GRCh38 chr3: 9,115,607-13,898,149 , GRCh37.p13 chr3: 9,157,291-13,939,646 MKRN2OS, RAF1, 106 more genes
    nsv6367022copy number variation1nstd223human GRCh38 chr3: 10,302,844-10,303,453 , GRCh37.p13 chr3: 10,344,528-10,345,137 SEC13
    nsv6311883copy number variation1nstd102humanUncertain significance GRCh37 chr3: 7,782,024-11,078,652 , GRCh38.p12 chr3: 7,740,337-11,036,966 CIDECP1, LMCD1, 71 more genes
    nsv6135258copy number variation1nstd213human GRCh37 chr3: 9,900,000-10,780,001 , GRCh38.p12 chr3: 9,858,316-10,738,316 ATP2B2, FANCD2, 29 more genes
    nsv6042788insertion1nstd212human GRCh38 chr3: 10,305,930-10,305,930 , GRCh37.p13 chr3: 10,347,614-10,347,614 SEC13
    nsv5995049copy number variation1nstd212human GRCh38 chr3: 9,995,584-11,870,473 , GRCh37.p13 chr3: 10,037,268-11,911,947 , VHL, 35 more genes
    nsv5990783copy number variation1nstd212human GRCh38 chr3: 10,050,341-11,870,472 , GRCh37.p13 chr3: 10,092,025-11,911,946 , SLC6A1, 29 more genes
    nsv5990720copy number variation1nstd212human GRCh38 chr3: 10,319,764-10,319,825 , GRCh37.p13 chr3: 10,361,448-10,361,509 SEC13
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