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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096827copy number variation1nstd102humanUncertain significance GRCh37 chr4: 110,772,640-110,773,152 , GRCh38.p12 chr4: 109,851,484-109,851,996 LRIT3
    nsv7054431inversion1nstd229human GRCh38 chr4: 108,267,754-117,667,771 , GRCh37.p13 chr4: 109,188,910-118,588,926 , MIR297, 128 more genes
    nsv6756725copy number variation1nstd229human GRCh38 chr4: 109,861,840-109,862,350 , GRCh37.p13 chr4: 110,782,996-110,783,506 LRIT3
    nsv6755674copy number variation1nstd229human GRCh38 chr4: 109,847,487-109,847,608 , GRCh37.p13 chr4: 110,768,643-110,768,764 LRIT3
    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
    nsv6572140inversion1nstd223human GRCh38 chr4: 108,267,752-117,667,773 , GRCh37.p13 chr4: 109,188,908-118,588,928 , RPS26P25, 128 more genes
    nsv6556222inversion1nstd223human GRCh38 chr4: 108,711,905-115,978,756 , GRCh37.p13 chr4: 109,633,061-116,899,912 , MIR577, 98 more genes
    nsv6391614copy number variation1nstd223human GRCh38 chr4: 109,868,393-109,914,666 , GRCh37.p13 chr4: 110,789,549-110,835,822 EGF, LRIT3, 1 more genes
    nsv6390992copy number variation1nstd223human GRCh38 chr4: 109,847,485-109,847,608 , GRCh37.p13 chr4: 110,768,641-110,768,764 LRIT3
    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
    nsv6292132mobile element insertion1nstd186human GRCh37 chr4: 110,783,329-110,783,380 , GRCh38.p12 chr4: 109,862,173-109,862,224 LRIT3
    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
    nsv6263765copy number variation1nstd214human GRCh38 chr4: 109,847,485-109,847,607 , GRCh37.p13 chr4: 110,768,641-110,768,763 LRIT3
    nsv6255141mobile element insertion1nstd215human GRCh38 chr4: 109,862,173-109,862,173 , GRCh37.p13 chr4: 110,783,329-110,783,329 LRIT3
    nsv6221291insertion1nstd214human GRCh38 chr4: 109,850,354-109,850,354 , GRCh37.p13 chr4: 110,771,510-110,771,510 LRIT3
    nsv6215290insertion1nstd214human GRCh38 chr4: 109,850,366-109,850,366 , GRCh37.p13 chr4: 110,771,522-110,771,522 LRIT3
    nsv6212431insertion1nstd214human GRCh38 chr4: 109,850,402-109,850,402 , GRCh37.p13 chr4: 110,771,558-110,771,558 LRIT3
    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
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