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Items: 1 to 20 of 211

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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
    nsv7066723inversion1nstd229human GRCh38 chr11: 129,437,269-129,726,123 , GRCh37.p13 chr11: 129,307,164-129,596,018 BARX2, LINC01395, 1 more genes
    nsv6911097copy number variation1nstd229human GRCh38 chr11: 129,611,339-129,613,894 , GRCh37.p13 chr11: 129,481,234-129,483,789 LINC01395
    nsv6901440copy number variation1nstd229human GRCh38 chr11: 129,615,639-129,615,846 , GRCh37.p13 chr11: 129,485,534-129,485,741 LINC01395
    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
    nsv6457816copy number variation1nstd223human GRCh38 chr11: 129,615,638-129,615,845 , GRCh37.p13 chr11: 129,485,533-129,485,740 LINC01395
    nsv6455831copy number variation1nstd223human GRCh38 chr11: 129,572,806-129,650,208 , GRCh37.p13 chr11: 129,442,701-129,520,103 LINC01395
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315090copy number variation1nstd102humanPathogenic GRCh37 chr11: 128,634,685-134,257,741 , GRCh38.p12 chr11: 128,764,790-134,387,847 BAK1P2, RN7SL167P, 73 more genes
    nsv6303203copy number variation1nstd186human GRCh37 chr11: 129,442,259-129,520,259 , GRCh38.p12 chr11: 129,572,364-129,650,364 LINC01395
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6132350copy number variation1nstd213human GRCh37 chr11: 128,570,000-130,240,001 , GRCh38.p12 chr11: 128,700,105-130,370,106 KCNJ1, ZBTB44, 28 more genes
    nsv6132094copy number variation1nstd213human GRCh37 chr11: 129,370,000-129,690,001 , GRCh38.p12 chr11: 129,500,105-129,820,106 TMEM45B, RPS27P20, 1 more genes
    nsv5511582copy number variation1nstd206human GRCh38 chr11: 129,572,364-129,650,364 , GRCh37.p13 chr11: 129,442,259-129,520,259 LINC01395
    nsv5495861copy number variation1nstd206human GRCh38 chr11: 129,615,638-129,615,845 , GRCh37.p13 chr11: 129,485,533-129,485,740 LINC01395
    nsv5348430translocation1nstd200human GRCh38 chr11: 129,615,638-129,615,638 , GRCh38 chr11: 129,615,845-129,615,845 , GRCh37.p13 chr11: 129,485,740-129,485,740 , GRCh37.p13 chr11: 129,485,533-129,485,533 LINC01395
    nsv5340795translocation1nstd200human GRCh37 chr11: 129,485,740-129,485,740 , GRCh37 chr11: 129,485,533-129,485,533 , GRCh38.p12 chr11: 129,615,638-129,615,638 , GRCh38.p12 chr11: 129,615,845-129,615,845 LINC01395
    nsv5319168copy number variation1nstd204human GRCh38.p13 chr11: 129,572,779-129,650,212 , GRCh37.p13 chr11: 129,442,674-129,520,107 LINC01395
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