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Items: 1 to 20 of 185

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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
    nsv6754257copy number variation1nstd229human GRCh38 chr4: 109,431,701-109,433,500 , GRCh37.p13 chr4: 110,352,857-110,354,656 SEC24B, SEC24B-AS1
    nsv6753308copy number variation1nstd229human GRCh38 chr4: 109,234,672-109,474,012 , GRCh37.p13 chr4: 110,155,828-110,395,168 SEC24B-AS1, COL25A1, 4 more genes
    nsv6749849copy number variation1nstd229human GRCh38 chr4: 103,966,147-109,668,724 , GRCh37.p13 chr4: 104,887,304-110,589,880 CYP2U1-AS1, OSTC, 66 more genes
    nsv6745689copy number variation1nstd229human GRCh38 chr4: 109,032,502-109,484,409 , GRCh37.p13 chr4: 109,953,658-110,405,565 SEC24B, COL25A1-DT, 4 more genes
    nsv6741226copy number variation1nstd229human GRCh38 chr4: 109,430,538-109,433,227 , GRCh37.p13 chr4: 110,351,694-110,354,383 SEC24B-AS1, SEC24B
    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
    nsv6392692copy number variation1nstd223human GRCh38 chr4: 109,234,672-109,474,012 , GRCh37.p13 chr4: 110,155,828-110,395,168 COL25A1-DT, SEC24B, 4 more genes
    nsv6381784copy number variation1nstd223human GRCh38 chr4: 109,032,502-109,484,409 , GRCh37.p13 chr4: 109,953,658-110,405,565 COL25A1, SEC24B, 4 more genes
    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
    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
    nsv5560513sequence alteration1nstd206human GRCh38 chr4: 108,640,149-109,466,577 , GRCh37.p13 chr4: 109,561,305-110,387,733 , RCC2P8, 10 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
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