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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
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7071514inversion1nstd229human GRCh38 chr11: 67,656,060-67,862,553 , GRCh37.p13 chr11: 67,423,531-67,630,024 ENPP7P7, OR7E145P, 8 more genes
    nsv7063416inversion1nstd229human GRCh38 chr11: 67,577,505-68,052,740 , GRCh37.p13 chr11: 67,344,976-67,820,207 ALDH3B1, FAM86C2P, 30 more genes
    nsv6912757copy number variation1nstd229human GRCh38 chr11: 66,793,001-68,121,500 , GRCh37.p13 chr11: 66,560,472-67,888,967 CHKA-DT, LOC107984341, 66 more genes
    nsv6911763copy number variation1nstd229human GRCh38 chr11: 67,577,408-68,033,450 , GRCh37.p13 chr11: 67,344,879-67,800,917 LINC02754, LOC112268076, 27 more genes
    nsv6911508copy number variation1nstd229human GRCh38 chr11: 67,541,590-68,051,961 , GRCh37.p13 chr11: 67,309,061-67,819,428 NDUFV1, ENPP7P7, 30 more genes
    nsv6907533copy number variation1nstd229human GRCh38 chr11: 67,683,455-67,689,695 , GRCh37.p13 chr11: 67,450,926-67,457,166 RPL37P2
    nsv6906255copy number variation1nstd229human GRCh38 chr11: 67,675,982-67,681,460 , GRCh37.p13 chr11: 67,443,453-67,448,931 ALDH3B2, RPL37P2
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6901523copy number variation1nstd229human GRCh38 chr11: 67,577,616-67,989,511 , GRCh37.p13 chr11: 67,345,087-67,756,982 EVA1CP4, LINC02754, 23 more genes
    nsv6621011copy number variation1nstd224human GRCh37 chr11: 67,402,374-67,616,520 , GRCh38.p12 chr11: 67,634,903-67,849,049 OR7E11P, ALG1L8P, 10 more genes
    nsv6459128copy number variation1nstd223human GRCh38 chr11: 67,577,616-67,989,511 , GRCh37.p13 chr11: 67,345,087-67,756,982 OR7E11P, UNC93B1, 23 more genes
    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
    nsv6132115copy number variation1nstd213human GRCh37 chr11: 67,280,000-68,040,001 , GRCh38.p12 chr11: 67,512,529-68,272,533 C11orf24, DOC2GP, 35 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5509313copy number variation1nstd206human GRCh38 chr11: 67,683,431-67,683,593 , GRCh37.p13 chr11: 67,450,902-67,451,064 RPL37P2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5275203copy number variation1nstd204human GRCh38.p13 chr11: 66,946,001-67,700,500 , GRCh37.p13 chr11: 66,713,472-67,467,971 , PC, 38 more genes
    nsv5120794mobile element insertion1nstd203human GRCh38 chr11: 67,681,677-67,681,690 , GRCh37.p13 chr11: 67,449,148-67,449,161 RPL37P2, ALDH3B2
    nsv4985094copy number variation1nstd200human GRCh38 chr11: 67,577,565-67,989,543 , GRCh37.p13 chr11: 67,345,036-67,757,014 , RNU6-46P, 24 more genes
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