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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv6916934copy number variation1nstd229human GRCh38 chr11: 130,377,626-130,839,160 , GRCh37.p13 chr11: 130,247,521-130,709,055 LOC105369575, MIR8052, 8 more genes
    nsv6916014copy number variation1nstd229human GRCh38 chr11: 130,693,673-130,703,581 , GRCh37.p13 chr11: 130,563,568-130,573,476 LINC02873
    nsv6915697copy number variation1nstd229human GRCh38 chr11: 130,714,988-130,715,282 , GRCh37.p13 chr11: 130,584,883-130,585,177 LINC02873
    nsv6914995copy number variation1nstd229human GRCh38 chr11: 130,698,420-130,698,580 , GRCh37.p13 chr11: 130,568,315-130,568,475 LINC02873
    nsv6911702copy number variation1nstd229human GRCh38 chr11: 130,630,079-130,673,094 , GRCh37.p13 chr11: 130,499,974-130,542,989 LINC02873, MIR8052
    nsv6911487copy number variation1nstd229human GRCh38 chr11: 130,553,739-131,533,260 , GRCh37.p13 chr11: 130,423,634-131,403,154 LOC105369579, LOC107984412, 15 more genes
    nsv6909675copy number variation1nstd229human GRCh38 chr11: 130,704,550-130,704,588 , GRCh37.p13 chr11: 130,574,445-130,574,483 LINC02873
    nsv6898849copy number variation1nstd229human GRCh38 chr11: 130,706,801-130,714,100 , GRCh37.p13 chr11: 130,576,696-130,583,995 LINC02873
    nsv6898223copy number variation1nstd229human GRCh38 chr11: 130,684,901-130,691,200 , GRCh37.p13 chr11: 130,554,796-130,561,095 LINC02873
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6634467copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 127,074,235-135,006,516 , GRCh38.p12 chr11: 127,204,340-135,076,622 APLP2, BAK1P2, 98 more genes
    nsv6470349copy number variation1nstd223human GRCh38 chr11: 130,700,392-130,700,922 , GRCh37.p13 chr11: 130,570,287-130,570,817 LINC02873
    nsv6467315copy number variation1nstd223human GRCh38 chr11: 130,553,739-131,533,260 , GRCh37.p13 chr11: 130,423,634-131,403,154 LOC105369577, LOC105369574, 15 more genes
    nsv6466038copy number variation1nstd223human GRCh38 chr11: 130,688,168-130,688,609 , GRCh37.p13 chr11: 130,558,063-130,558,504 LINC02873
    nsv6462284copy number variation1nstd223human GRCh38 chr11: 130,563,109-131,175,248 , GRCh37.p13 chr11: 130,433,004-131,045,143 LOC105369577, PPP1R10P1, 10 more genes
    nsv6458954copy number variation1nstd223human GRCh38 chr11: 130,684,901-130,685,500 , GRCh37.p13 chr11: 130,554,796-130,555,395 LINC02873
    nsv6458174copy number variation1nstd223human GRCh38 chr11: 130,685,001-130,686,700 , GRCh37.p13 chr11: 130,554,896-130,556,595 LINC02873
    nsv6457482copy number variation1nstd223human GRCh38 chr11: 130,704,549-130,704,586 , GRCh37.p13 chr11: 130,574,444-130,574,481 LINC02873
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