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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099298copy number variation1nstd231human GRCh38.p12 chr1: 68,115,402-81,183,740 , GRCh37 chr1: 68,581,085-81,649,425 ACADM, COX6A1P1, 145 more genes
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7052659inversion1nstd229human GRCh38 chr1: 74,719,278-75,909,786 , GRCh37.p13 chr1: 75,184,962-76,375,471 RNU6-503P, LOC100422213, 14 more genes
    nsv7047632inversion1nstd229human GRCh38 chr1: 74,160,663-78,762,216 , GRCh37.p13 chr1: 74,626,347-79,227,901 SLC44A5, MGC27382, 66 more genes
    nsv6654699copy number variation1nstd229human GRCh38 chr1: 75,787,801-75,798,600 , GRCh37.p13 chr1: 76,253,486-76,264,285 SNORD45B, SNORD45A, 2 more genes
    nsv6654690copy number variation1nstd229human GRCh38 chr1: 75,468,583-76,252,770 , GRCh37.p13 chr1: 75,934,268-76,718,455 RPL29P5, LOC105378806, 14 more genes
    nsv6654685copy number variation1nstd229human GRCh38 chr1: 75,362,831-75,919,055 , GRCh37.p13 chr1: 75,828,516-76,384,740 SNORD45B, SNORD45C, 11 more genes
    nsv6654126copy number variation1nstd229human GRCh38 chr1: 72,916,807-75,896,360 , GRCh37.p13 chr1: 73,382,490-76,362,045 LOC105378801, LRRIQ3, 31 more genes
    nsv6626281copy number variation1nstd224human GRCh37 chr1: 74,166,048-77,951,148 , GRCh38.p12 chr1: 73,700,365-77,485,463 ACADM, CRYZ, 41 more genes
    nsv6541951inversion1nstd223human GRCh38 chr1: 74,719,278-75,909,781 , GRCh37.p13 chr1: 75,184,962-76,375,466 RABGGTB, TYW3, 14 more genes
    nsv6322664copy number variation1nstd223human GRCh38 chr1: 75,776,896-75,804,283 , GRCh37.p13 chr1: 76,242,581-76,269,968 SNORD45B, MSH4, 3 more genes
    nsv6319391copy number variation1nstd223human GRCh38 chr1: 75,646,330-79,015,520 , GRCh37.p13 chr1: 76,112,015-79,481,205 ADGRL4, IFI44, 52 more genes
    nsv6315306copy number variation1nstd102humanUncertain significance GRCh38 chr1: 66,885,559-77,949,895 , GRCh37.p13 chr1: 67,351,242-78,415,580 DNAJB6P4, LRRC7, 137 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RNA5SP51, ADGRL4, 315 more genes
    nsv5431614copy number variation1nstd206human GRCh38 chr1: 75,608,610-75,913,087 , GRCh37.p13 chr1: 76,074,295-76,378,772 ACADM, DLSTP1, 7 more genes
    nsv5353092translocation1nstd200human GRCh38 chr1: 75,789,430-75,789,430 , GRCh38 chr7: 151,969,577-151,969,577 , GRCh37.p13 chr1: 76,255,115-76,255,115 , GRCh37.p13 chr7: 151,666,662-151,666,662 RABGGTB, SNORD45B, 1 more genes
    nsv5343654translocation1nstd200human GRCh37 chr1: 76,255,523-76,255,523 , GRCh37 chr7: 151,666,665-151,666,665 , GRCh38.p12 chr1: 75,789,838-75,789,838 , GRCh38.p12 chr7: 151,969,580-151,969,580 RABGGTB, SNORD45B, 1 more genes
    nsv5329803translocation1nstd200human GRCh37 chr1: 76,255,115-76,255,115 , GRCh37 chr7: 151,666,662-151,666,662 , GRCh38.p12 chr1: 75,789,430-75,789,430 , GRCh38.p12 chr7: 151,969,577-151,969,577 RABGGTB, SNORD45B, 1 more genes
    nsv5324779translocation1nstd204human GRCh37.p13 chr7: 151,666,662-151,666,662 , GRCh38.p13 chr7: 151,969,577-151,969,577 , GRCh38.p13 chr1: 75,789,430-75,789,430 , GRCh37.p13 chr1: 76,255,115-76,255,115 RABGGTB, SNORD45B, 1 more genes
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
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