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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139694copy number variation1nstd232human GRCh37.p13 chr4: 110,748,458-110,748,523 , GRCh38.p12 chr4: 109,827,302-109,827,367 RRH
    nsv7054431inversion1nstd229human GRCh38 chr4: 108,267,754-117,667,771 , GRCh37.p13 chr4: 109,188,910-118,588,926 , MIR297, 128 more genes
    nsv6745079copy number variation1nstd229human GRCh38 chr4: 109,839,468-109,886,708 , GRCh37.p13 chr4: 110,760,624-110,807,864 KRT19P3, RRH, 1 more genes
    nsv6738492copy number variation1nstd229human GRCh38 chr4: 109,827,304-109,827,368 , GRCh37.p13 chr4: 110,748,460-110,748,524 RRH
    nsv6572140inversion1nstd223human GRCh38 chr4: 108,267,752-117,667,773 , GRCh37.p13 chr4: 109,188,908-118,588,928 , RPS26P25, 128 more genes
    nsv6564921inversion1nstd223human GRCh38 chr4: 109,841,074-109,841,892 , GRCh37.p13 chr4: 110,762,230-110,763,048 RRH
    nsv6556222inversion1nstd223human GRCh38 chr4: 108,711,905-115,978,756 , GRCh37.p13 chr4: 109,633,061-116,899,912 , MIR577, 98 more genes
    nsv6384058copy number variation1nstd223human GRCh38 chr4: 109,830,297-109,831,175 , GRCh37.p13 chr4: 110,751,453-110,752,331 RRH
    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
    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
    nsv6153787copy number variation1nstd214human GRCh38 chr4: 109,827,302-109,827,367 , GRCh37.p13 chr4: 110,748,458-110,748,523 RRH
    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
    nsv5994610copy number variation1nstd212human GRCh38 chr4: 109,827,302-109,827,368 , GRCh37.p13 chr4: 110,748,458-110,748,524 RRH
    nsv5969033inversion1nstd209human GRCh38 chr4: 108,267,752-117,667,772 , GRCh37.p13 chr4: 109,188,908-118,588,927 , ANK2, 134 more genes
    nsv5948541insertion1nstd209human GRCh38 chr4: 109,839,042-109,839,042 , GRCh37.p13 chr4: 110,760,198-110,760,198 RRH
    nsv5894085copy number variation1nstd209human GRCh38 chr4: 109,827,302-109,827,367 , GRCh37.p13 chr4: 110,748,458-110,748,523 RRH
    nsv5724660mobile element insertion2nstd211human GRCh38 chr4: 109,839,053-109,839,053 , GRCh37.p13 chr4: 110,760,209-110,760,209 RRH
    nsv5605400insertion1nstd207human GRCh38 chr4: 109,839,042-109,839,042 , GRCh37.p13 chr4: 110,760,198-110,760,198 RRH
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