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Items: 1 to 20 of 388

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099225copy number variation1nstd231human GRCh38.p12 chr1: 111,381,594-114,553,029 , GRCh37 chr1: 111,924,216-115,095,650 ADORA3, RHOC, 74 more genes
    nsv7095696copy number variation1nstd102humanPathogenic GRCh37 chr1: 112,318,699-115,576,848 , GRCh38.p12 chr1: 111,776,077-115,034,227 AKR7A2P1, PTPN22, 69 more genes
    nsv7095695copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,145,905-114,454,813 , GRCh38.p12 chr1: 110,603,283-113,912,191 LOC107985189, RNU6-792P, 83 more genes
    nsv7053817inversion1nstd229human GRCh38 chr1: 112,472,093-113,188,421 , GRCh37.p13 chr1: 113,014,715-113,731,043 LOC107985189, NUTF2P4, 22 more genes
    nsv7049733inversion1nstd229human GRCh38 chr1: 112,595,027-113,169,871 , GRCh37.p13 chr1: 113,137,649-113,712,493 LRIG2, RLIMP2, 21 more genes
    nsv7047135inversion1nstd229human GRCh38 chr1: 112,389,397-113,355,432 , GRCh37.p13 chr1: 112,932,019-113,898,054 LRIG2-DT, PPM1J, 26 more genes
    nsv7046226inversion1nstd229human GRCh38 chr1: 112,507,311-113,213,376 , GRCh37.p13 chr1: 113,049,933-113,755,998 NUTF2P4, LINC01357, 24 more genes
    nsv7044503inversion1nstd229human GRCh38 chr1: 112,614,099-112,614,225 , GRCh37.p13 chr1: 113,156,721-113,156,847 ST7L
    nsv7038327inversion1nstd229human GRCh38 chr1: 112,559,726-112,570,323 , GRCh37.p13 chr1: 113,102,348-113,112,945 ST7L
    nsv6640310copy number variation1nstd229human GRCh38 chr1: 112,601,847-112,605,460 , GRCh37.p13 chr1: 113,144,469-113,148,082 ST7L
    nsv6640309copy number variation1nstd229human GRCh38 chr1: 112,599,500-112,886,283 , GRCh37.p13 chr1: 113,142,122-113,428,905 ST7L, LOC105378911, 12 more genes
    nsv6640085copy number variation1nstd229human GRCh38 chr1: 112,542,240-112,564,846 , GRCh37.p13 chr1: 113,084,862-113,107,468 ST7L
    nsv6640084copy number variation1nstd229human GRCh38 chr1: 112,526,683-112,534,019 , GRCh37.p13 chr1: 113,069,305-113,076,641 WNT2B, ST7L
    nsv6640082copy number variation1nstd229human GRCh38 chr1: 112,498,065-112,664,236 , GRCh37.p13 chr1: 113,040,687-113,206,858 CAPZA1, MRPL53P1, 3 more genes
    nsv6640081copy number variation1nstd229human GRCh38 chr1: 112,490,913-112,518,758 , GRCh37.p13 chr1: 113,033,535-113,061,380 ST7L, WNT2B
    nsv6639989copy number variation1nstd229human GRCh38 chr1: 112,619,026-113,203,602 , GRCh37.p13 chr1: 113,161,648-113,746,224 MOV10, RNU7-70P, 23 more genes
    nsv6639988copy number variation1nstd229human GRCh38 chr1: 112,598,398-112,610,790 , GRCh37.p13 chr1: 113,141,020-113,153,412 ST7L
    nsv6639987copy number variation1nstd229human GRCh38 chr1: 112,558,919-112,571,010 , GRCh37.p13 chr1: 113,101,541-113,113,632 ST7L
    nsv6639881copy number variation1nstd229human GRCh38 chr1: 112,604,101-112,609,800 , GRCh37.p13 chr1: 113,146,723-113,152,422 ST7L
    nsv6639879copy number variation1nstd229human GRCh38 chr1: 112,575,543-112,580,014 , GRCh37.p13 chr1: 113,118,165-113,122,636 ST7L
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