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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 PHF7, SEMA3G, 47 more genes
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv6711686copy number variation1nstd229human GRCh38 chr3: 51,850,901-52,533,900 , GRCh37.p13 chr3: 51,884,917-52,567,916 LOC105377088, GLYCTK-AS1, 37 more genes
    nsv6700890copy number variation1nstd229human GRCh38 chr3: 52,237,701-52,533,900 , GRCh37.p13 chr3: 52,271,717-52,567,916 STAB1, TWF2, 16 more genes
    nsv6538784inversion1nstd223human GRCh38 chr3: 52,252,325-52,252,888 , GRCh37.p13 chr3: 52,286,341-52,286,904 WDR82
    nsv6369827copy number variation1nstd223human GRCh38 chr3: 52,164,358-54,467,618 , GRCh37.p13 chr3: 52,198,374-54,501,645 SEMA3G, STAB1, 61 more genes
    nsv6359362copy number variation1nstd223human GRCh38 chr3: 52,278,201-52,278,800 , GRCh37.p13 chr3: 52,312,217-52,312,816 WDR82
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 more genes
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5686369mobile element insertion2nstd211human GRCh38 chr3: 52,267,864-52,267,864 , GRCh37.p13 chr3: 52,301,880-52,301,880 MIRLET7G, WDR82
    nsv5681026mobile element insertion1nstd211human GRCh38 chr3: 52,275,596-52,275,596 , GRCh37.p13 chr3: 52,309,612-52,309,612 WDR82
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5549536insertion1nstd206human GRCh38 chr3: 52,275,596-52,275,639 , GRCh37.p13 chr3: 52,309,612-52,309,655 WDR82
    nsv5401514mobile element insertion1nstd206human GRCh38 chr3: 52,267,864-52,267,915 , GRCh37.p13 chr3: 52,301,880-52,301,931 WDR82, MIRLET7G
    nsv5200746copy number variation1nstd204human GRCh38.p13 chr3: 52,056,901-52,406,800 , GRCh37.p13 chr3: 52,090,917-52,440,816 ALAS1, BAP1, 16 more genes
    nsv5079792mobile element insertion1nstd203human GRCh38 chr3: 52,254,726-52,254,739 , GRCh37.p13 chr3: 52,288,742-52,288,755 WDR82
    nsv5070815mobile element insertion1nstd203human GRCh38 chr3: 52,273,482-52,273,502 , GRCh37.p13 chr3: 52,307,498-52,307,518 WDR82
    nsv5062256mobile element insertion1nstd203human GRCh38 chr3: 52,275,588-52,275,596 , GRCh37.p13 chr3: 52,309,604-52,309,612 WDR82
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
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