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Items: 1 to 20 of 352

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951184insertion1nstd209human GRCh38 chr10: 95,908,767-95,908,767 , GRCh37.p13 chr10: 97,668,524-97,668,524 ENTPD1-AS1, CC2D2B
    nsv5949991insertion1nstd209human GRCh38 chr10: 95,947,083-95,947,083 , GRCh37.p13 chr10: 97,706,840-97,706,840 ENTPD1-AS1, CC2D2B
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5921696copy number variation1nstd209human GRCh38 chr10: 95,990,661-95,991,149 , GRCh37.p13 chr10: 97,750,418-97,750,906 ENTPD1-AS1, CC2D2B
    nsv5865187copy number variation1nstd209human GRCh38 chr10: 95,912,602-95,925,780 , GRCh37.p13 chr10: 97,672,359-97,685,537 CC2D2B, ENTPD1-AS1
    nsv5718059mobile element insertion2nstd211human GRCh38 chr10: 96,034,955-96,034,955 , GRCh37.p13 chr10: 97,794,712-97,794,712 CC2D2B, ENTPD1-AS1
    nsv5709057mobile element insertion1nstd211human GRCh38 chr10: 95,945,403-95,945,403 , GRCh37.p13 chr10: 97,705,160-97,705,160 ENTPD1-AS1, CC2D2B
    nsv5704189mobile element insertion2nstd211human GRCh38 chr10: 95,959,736-95,959,736 , GRCh37.p13 chr10: 97,719,493-97,719,493 ENTPD1-AS1, CC2D2B
    nsv5694465mobile element insertion2nstd211human GRCh38 chr10: 95,908,781-95,908,781 , GRCh37.p13 chr10: 97,668,538-97,668,538 ENTPD1-AS1, CC2D2B
    nsv5643208insertion1nstd207human GRCh38 chr10: 95,986,358-95,986,358 , GRCh37.p13 chr10: 97,746,115-97,746,115 ENTPD1-AS1, CC2D2B
    nsv5638160insertion1nstd207human GRCh38 chr10: 96,022,236-96,022,236 , GRCh37.p13 chr10: 97,781,993-97,781,993 ENTPD1-AS1, CC2D2B
    nsv5628399insertion1nstd207human GRCh38 chr10: 95,908,767-95,908,767 , GRCh37.p13 chr10: 97,668,524-97,668,524 CC2D2B, ENTPD1-AS1
    nsv5597929copy number variation1nstd207human GRCh38 chr10: 95,993,922-95,993,977 , GRCh37.p13 chr10: 97,753,679-97,753,734 CC2D2B, ENTPD1-AS1
    nsv5564286copy number variation1nstd102humanUncertain significance GRCh37 chr10: 97,366,499-98,031,175 , GRCh38.p12 chr10: 95,606,742-96,271,418 CCNJ, ENTPD1-AS1, 10 more genes
    nsv5551645insertion1nstd206human GRCh38 chr10: 96,009,540-96,009,578 , GRCh37.p13 chr10: 97,769,297-97,769,335 CC2D2B, ENTPD1-AS1
    nsv5484106copy number variation1nstd206human GRCh38 chr10: 95,948,320-95,949,869 , GRCh37.p13 chr10: 97,708,077-97,709,626 ENTPD1-AS1, CC2D2B
    nsv5481299copy number variation1nstd206human GRCh38 chr10: 95,949,200-96,035,000 , GRCh37.p13 chr10: 97,708,957-97,794,757 RPL21P90, ENTPD1-AS1, 1 more genes
    nsv5413332mobile element insertion1nstd206human GRCh38 chr10: 95,945,403-95,945,454 , GRCh37.p13 chr10: 97,705,160-97,705,211 ENTPD1-AS1, CC2D2B
    nsv5407022mobile element insertion1nstd206human GRCh38 chr10: 95,908,767-95,908,767 , GRCh37.p13 chr10: 97,668,524-97,668,524 CC2D2B, ENTPD1-AS1
    nsv5199078mobile element insertion1nstd203human GRCh38 chr10: 96,027,628-96,027,635 , GRCh37.p13 chr10: 97,787,385-97,787,392 ENTPD1-AS1, CC2D2B
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