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Items: 1 to 20 of 183

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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
    nsv7045556inversion1nstd229human GRCh38 chr4: 110,351,226-111,944,789 , GRCh37.p13 chr4: 111,272,382-112,865,945 , PITX2, 14 more genes
    nsv6756583copy number variation1nstd229human GRCh38 chr4: 110,624,350-110,624,421 , GRCh37.p13 chr4: 111,545,506-111,545,577 PITX2
    nsv6756192copy number variation1nstd229human GRCh38 chr4: 110,612,401-110,617,000 , GRCh37.p13 chr4: 111,533,557-111,538,156 LOC105377363, PANCR, 1 more genes
    nsv6749616copy number variation1nstd229human GRCh38 chr4: 110,331,263-110,664,774 , GRCh37.p13 chr4: 111,252,419-111,585,930 ENPEP, RPL7L1P13, 5 more genes
    nsv6742506copy number variation1nstd229human GRCh38 chr4: 110,638,299-110,638,355 , GRCh37.p13 chr4: 111,559,455-111,559,511 PITX2
    nsv6741900copy number variation1nstd229human GRCh38 chr4: 110,613,357-110,621,199 , GRCh37.p13 chr4: 111,534,513-111,542,355 PANCR, PITX2, 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
    nsv6562953inversion1nstd223human GRCh38 chr4: 110,596,046-110,898,650 , GRCh37.p13 chr4: 111,517,202-111,819,806 PITX2, MIR297, 2 more genes
    nsv6556222inversion1nstd223human GRCh38 chr4: 108,711,905-115,978,756 , GRCh37.p13 chr4: 109,633,061-116,899,912 , MIR577, 98 more genes
    nsv6380669copy number variation1nstd223human GRCh38 chr4: 110,494,660-110,898,741 , GRCh37.p13 chr4: 111,415,816-111,819,897 PANCR, PITX2, 3 more genes
    nsv6375972copy number variation1nstd223human GRCh38 chr4: 110,638,295-110,638,355 , GRCh37.p13 chr4: 111,559,451-111,559,511 PITX2
    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
    nsv6311706copy number variation1nstd102humanPathogenic GRCh37 chr4: 111,539,281-111,554,154 , GRCh38.p12 chr4: 110,618,125-110,632,998 PITX2
    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
    nsv6162137copy number variation1nstd214human GRCh38 chr4: 110,638,295-110,638,354 , GRCh37.p13 chr4: 111,559,451-111,559,510 PITX2
    nsv6153101copy number variation1nstd214human GRCh38 chr4: 110,624,350-110,624,420 , GRCh37.p13 chr4: 111,545,506-111,545,576 PITX2
    nsv6135272copy number variation1nstd213human GRCh37 chr4: 111,480,000-111,620,001 , GRCh38.p12 chr4: 110,558,844-110,698,845 ENPEP, PITX2, 2 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
    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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