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Items: 1 to 20 of 270

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914717copy number variation1nstd209human GRCh38 chr7: 2,549,793-2,549,946 , GRCh37.p13 chr7: 2,589,427-2,589,580 BRAT1
    nsv5674031copy number variation1nstd102humanPathogenic GRCh37 chr7: 2,584,533-2,594,065 , GRCh38.p12 chr7: 2,544,899-2,554,431 BRAT1
    nsv5564496copy number variation1nstd102humanPathogenic GRCh37 chr7: 2,559,496-2,594,065 , GRCh38.p12 chr7: 2,519,862-2,554,431 BRAT1, LFNG, 1 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5363614translocation1nstd200human GRCh38 chr7: 2,542,170-2,542,170 , GRCh38 chr7: 2,542,627-2,542,627 , GRCh37.p13 chr7: 2,581,804-2,581,804 , GRCh37.p13 chr7: 2,582,261-2,582,261 BRAT1
    nsv5363613translocation1nstd200human GRCh38 chr7: 2,542,150-2,542,150 , GRCh38 chr7: 2,542,886-2,542,886 , GRCh37.p13 chr7: 2,581,784-2,581,784 , GRCh37.p13 chr7: 2,582,520-2,582,520 BRAT1
    nsv5312115copy number variation1nstd204human GRCh38.p13 chr7: 2,343,227-2,650,512 , GRCh37.p13 chr7: 2,382,862-2,690,146 , LOC107986759, 12 more genes
    nsv5235186copy number variation1nstd204human GRCh38.p13 chr7: 2,536,701-2,583,700 , GRCh37.p13 chr7: 2,576,335-2,623,334 BRAT1, IQCE
    nsv5229707copy number variation1nstd204human GRCh38.p13 chr7: 2,511,785-2,551,762 , GRCh37.p13 chr7: 2,551,419-2,591,396 BRAT1, MIR4648, 1 more genes
    nsv5223549copy number variation1nstd204human GRCh38.p13 chr7: 2,552,226-2,604,816 , GRCh37.p13 chr7: 2,591,860-2,644,450 IQCE, BRAT1
    nsv5115525mobile element insertion1nstd203human GRCh38 chr7: 2,550,467-2,550,508 , GRCh37.p13 chr7: 2,590,101-2,590,142 BRAT1
    nsv5111777mobile element insertion1nstd203human GRCh38 chr7: 2,550,457-2,550,508 , GRCh37.p13 chr7: 2,590,091-2,590,142 BRAT1
    nsv5108034mobile element insertion1nstd203human GRCh38 chr7: 2,550,508-2,550,508 , GRCh37.p13 chr7: 2,590,142-2,590,142 BRAT1
    nsv4953218copy number variation1nstd200human GRCh38 chr7: 2,029,930-2,586,635 , GRCh37.p13 chr7: 2,069,565-2,626,269 , NGRNP3, 18 more genes
    nsv4949620copy number variation1nstd200human GRCh38 chr7: 2,514,358-2,539,393 , GRCh37.p13 chr7: 2,553,992-2,579,027 MIR4648, LFNG, 1 more genes
    nsv4949613copy number variation1nstd200human GRCh38 chr7: 2,418,114-2,573,409 , GRCh37.p13 chr7: 2,457,749-2,613,043 , LFNG, 6 more genes
    nsv4824990copy number variation1nstd200human GRCh37 chr7: 2,589,427-2,589,582 , GRCh38.p12 chr7: 2,549,793-2,549,948 BRAT1
    nsv4824985copy number variation1nstd200human GRCh37 chr7: 2,383,064-2,689,799 , GRCh38.p12 chr7: 2,343,429-2,650,165 , LFNG, 12 more genes
    nsv4824978copy number variation1nstd200human GRCh37 chr7: 2,069,565-2,626,269 , GRCh38.p12 chr7: 2,029,930-2,586,635 , SNORA114, 18 more genes
    nsv4818354copy number variation1nstd200human GRCh37 chr7: 2,587,406-2,587,486 , GRCh38.p12 chr7: 2,547,772-2,547,852 BRAT1
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