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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4940470copy number variation1nstd200human GRCh38 chr6: 26,202,619-26,216,555 , GRCh37.p13 chr6: 26,202,847-26,216,783 H2AC8, H4C5, 2 more genes
    nsv4934536copy number variation1nstd200human GRCh38 chr6: 26,150,781-26,331,570 , GRCh37.p13 chr6: 26,151,009-26,331,798 , LARP1P1, 41 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4828555copy number variation1nstd200human GRCh37 chr6: 26,213,044-26,216,377 , GRCh38.p12 chr6: 26,212,816-26,216,149 H2BC8, H2AC8
    nsv4815680copy number variation1nstd200human GRCh37 chr6: 26,202,847-26,216,783 , GRCh38.p12 chr6: 26,202,619-26,216,555 H2BC8, H2AC8, 2 more genes
    nsv4729341copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,046,566-26,670,193 , GRCh38.p12 chr6: 26,046,338-26,669,965 H1-4, TRV-CAC1-6, 78 more genes
    nsv4728787copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,090,243-26,265,667 , GRCh38.p12 chr6: 26,090,015-26,265,439 H2AC7, H2AC9P, 26 more genes
    nsv4598439copy number variation1nstd183human GRCh37 chr6: 26,153,284-26,235,966 , GRCh38.p12 chr6: 26,153,056-26,235,738 H1-3, H2BC7, 15 more genes
    nsv4598438copy number variation1nstd183human GRCh37 chr6: 26,103,998-26,365,563 , GRCh38.p12 chr6: 26,103,770-26,365,335 , H2AC10P, 46 more genes
    nsv4593441copy number variation1nstd183human GRCh37 chr6: 26,153,284-26,321,490 , GRCh38.p12 chr6: 26,153,056-26,321,262 , H2BC9, 35 more genes
    nsv4592078copy number variation1nstd183human GRCh37 chr6: 26,189,288-26,217,801 , GRCh38.p12 chr6: 26,189,060-26,217,573 H2AC8, RPS10P1, 8 more genes
    nsv4592077copy number variation1nstd183human GRCh37 chr6: 26,171,332-26,232,837 , GRCh38.p12 chr6: 26,171,104-26,232,609 H2BC5, H2BC6, 13 more genes
    nsv4456351copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,896,585-26,287,389 , GRCh38.p12 chr6: 25,896,357-26,287,161 H3P26, H1-6, 44 more genes
    nsv4455820copy number variation1nstd102humanUncertain significance GRCh37 chr6: 25,996,066-26,303,969 , GRCh38.p12 chr6: 25,995,838-26,303,741 H4C6, H4C3, 44 more genes
    nsv4455529copy number variation1nstd102humanUncertain significance GRCh37 chr6: 26,067,580-26,306,202 , GRCh38.p12 chr6: 26,067,352-26,305,974 RPS10P1, H1-12P, 33 more genes
    nsv4375795copy number variation1nstd173human GRCh37 chr6: 26,207,758-26,303,178 , GRCh38.p12 chr6: 26,207,530-26,302,950 , H1-3, 16 more genes
    nsv4374516copy number variation1nstd173human GRCh37 chr6: 26,128,446-26,856,189 , GRCh38.p12 chr6: 26,128,218-26,888,410 , H3C8, 85 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3920471copy number variation1nstd102humanLikely benign GRCh37 chr6: 25,991,630-26,280,921 , NCBI36 chr6: 26,099,609-26,388,900 , GRCh38 chr6: 25,991,402-26,280,693 H2AC8, H2BC8, 41 more genes
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