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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054431inversion1nstd229human GRCh38 chr4: 108,267,754-117,667,771 , GRCh37.p13 chr4: 109,188,910-118,588,926 , MIR297, 128 more genes
    nsv6757110copy number variation1nstd229human GRCh38 chr4: 109,703,530-109,707,751 , GRCh37.p13 chr4: 110,624,686-110,628,907 CASP6
    nsv6754253copy number variation1nstd229human GRCh38 chr4: 109,703,519-109,704,065 , GRCh37.p13 chr4: 110,624,675-110,625,221 CASP6
    nsv6747919copy number variation1nstd229human GRCh38 chr4: 109,696,955-109,697,566 , GRCh37.p13 chr4: 110,618,111-110,618,722 CASP6
    nsv6572140inversion1nstd223human GRCh38 chr4: 108,267,752-117,667,773 , GRCh37.p13 chr4: 109,188,908-118,588,928 , RPS26P25, 128 more genes
    nsv6565282inversion1nstd223human GRCh38 chr4: 109,695,475-109,696,770 , GRCh37.p13 chr4: 110,616,631-110,617,926 CASP6
    nsv6556222inversion1nstd223human GRCh38 chr4: 108,711,905-115,978,756 , GRCh37.p13 chr4: 109,633,061-116,899,912 , MIR577, 98 more genes
    nsv6395418copy number variation1nstd223human GRCh38 chr4: 109,701,801-109,705,800 , GRCh37.p13 chr4: 110,622,957-110,626,956 CASP6
    nsv6385288copy number variation1nstd223human GRCh38 chr4: 109,691,190-109,691,947 , GRCh37.p13 chr4: 110,612,346-110,613,103 CASP6
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6298048copy number variation1nstd186human GRCh37 chr4: 110,621,904-110,621,999 , GRCh38.p12 chr4: 109,700,748-109,700,843 CASP6
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134883copy number variation1nstd213human GRCh37 chr4: 107,930,000-111,020,001 , GRCh38.p12 chr4: 107,008,843-110,098,845 CASP6, EGF, 46 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv5969033inversion1nstd209human GRCh38 chr4: 108,267,752-117,667,772 , GRCh37.p13 chr4: 109,188,908-118,588,927 , ANK2, 134 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5471174copy number variation1nstd206human GRCh38 chr4: 109,700,748-109,700,843 , GRCh37.p13 chr4: 110,621,904-110,621,999 CASP6
    nsv5367751translocation1nstd200human GRCh38 chr4: 109,697,619-109,697,619 , GRCh38 chr4: 109,694,700-109,694,700 , GRCh37.p13 chr4: 110,618,775-110,618,775 , GRCh37.p13 chr4: 110,615,856-110,615,856 CASP6
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