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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077246inversion1nstd229human GRCh38 chr15: 64,487,767-67,498,498 , GRCh37.p13 chr15: 64,779,966-67,790,836 LETM1P1, MIR4512, 74 more genes
    nsv7063733inversion1nstd229human GRCh38 chr15: 63,479,684-65,571,065 , GRCh37.p13 chr15: 63,771,883-65,863,403 TRIP4, RNU5B-1, 45 more genes
    nsv6976386copy number variation1nstd229human GRCh38 chr15: 64,792,594-64,814,007 , GRCh37.p13 chr15: 65,084,793-65,106,206 PIF1
    nsv6968187copy number variation1nstd229human GRCh38 chr15: 64,789,473-64,823,539 , GRCh37.p13 chr15: 65,081,672-65,115,738 PIF1
    nsv6964677copy number variation1nstd229human GRCh38 chr15: 64,789,595-64,816,937 , GRCh37.p13 chr15: 65,081,794-65,109,136 PIF1
    nsv6961994copy number variation1nstd229human GRCh38 chr15: 64,811,514-64,834,981 , GRCh37.p13 chr15: 65,103,713-65,127,180 PIF1
    nsv6961733copy number variation1nstd229human GRCh38 chr15: 64,791,202-64,835,377 , GRCh37.p13 chr15: 65,083,401-65,127,576 PIF1
    nsv6511855copy number variation1nstd223human GRCh38 chr15: 64,785,544-64,821,992 , GRCh37.p13 chr15: 65,077,743-65,114,191 PIF1
    nsv6314072copy number variation1nstd102humanUncertain significance GRCh37 chr15: 64,978,681-65,679,053 , GRCh38.p12 chr15: 64,686,482-65,386,715 CLPX, RNU5B-1, 22 more genes
    nsv6133150copy number variation1nstd213human GRCh37 chr15: 59,870,000-66,270,001 , GRCh38.p12 chr15: 59,577,801-65,977,663 GTF2A2, OAZ2, 115 more genes
    nsv5526353copy number variation1nstd206human GRCh38 chr15: 64,815,341-64,837,137 , GRCh37.p13 chr15: 65,107,540-65,129,336 PIF1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5313789copy number variation1nstd204human GRCh38.p13 chr15: 64,796,021-64,822,935 , GRCh37.p13 chr15: 65,088,220-65,115,134 PIF1
    nsv5274729copy number variation1nstd204human GRCh38.p13 chr15: 64,796,101-64,822,900 , GRCh37.p13 chr15: 65,088,300-65,115,099 PIF1
    nsv5266115copy number variation1nstd204human GRCh38.p13 chr15: 64,817,344-64,818,676 , GRCh37.p13 chr15: 65,109,543-65,110,875 PIF1
    nsv5261486copy number variation1nstd204human GRCh38.p13 chr15: 64,819,477-64,820,976 , GRCh37.p13 chr15: 65,111,676-65,113,175 PIF1
    nsv4992017copy number variation1nstd200human GRCh38 chr15: 64,821,919-64,832,458 , GRCh37.p13 chr15: 65,114,118-65,124,657 PIF1
    nsv4849841copy number variation1nstd200human GRCh37 chr15: 65,088,244-65,115,112 , GRCh38.p12 chr15: 64,796,045-64,822,913 PIF1
    nsv4729193copy number variation1nstd102humanUncertain significance GRCh37 chr15: 64,705,736-65,178,188 , GRCh38.p12 chr15: 64,413,537-64,885,989 RBPMS2, GAPDHP61, 11 more genes
    nsv4384571copy number variation1nstd173human GRCh37 chr15: 65,096,792-65,258,596 , GRCh38.p12 chr15: 64,804,593-64,966,255 , ANKDD1A, 3 more genes
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