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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144783insertion1nstd232human GRCh37.p13 chr11: 67,379,040-67,379,040 , GRCh38.p12 chr11: 67,611,569-67,611,569 NDUFV1, DOC2GP
    nsv7136997copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 67,378,042-67,380,013 , GRCh38.p12 chr11: 67,610,571-67,612,542 NDUFV1, DOC2GP
    nsv7136943copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 67,377,107-67,380,013 , GRCh38.p12 chr11: 67,609,636-67,612,542 NDUFV1, DOC2GP
    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
    nsv7093938copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,351,315-67,379,929 , GRCh38.p12 chr11: 67,583,844-67,612,458 NDUFV1-DT, DOC2GP, 2 more genes
    nsv7073277inversion1nstd229human GRCh38 chr11: 67,611,042-67,611,228 , GRCh37.p13 chr11: 67,378,513-67,378,699 NDUFV1
    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
    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
    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
    nsv6458158copy number variation1nstd223human GRCh38 chr11: 67,612,777-67,615,169 , GRCh37.p13 chr11: 67,380,248-67,382,640 DOC2GP, NDUFV1
    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
    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
    nsv4985095copy number variation1nstd200human GRCh38 chr11: 67,578,495-67,641,726 , GRCh37.p13 chr11: 67,345,966-67,409,197 GSTP1, ACY3, 5 more genes
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