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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094099copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,759,017-68,216,538 , GRCh38.p12 chr11: 67,991,546-68,449,070 LRP5, UNC93B1, 11 more genes
    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
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv7068521inversion1nstd229human GRCh38 chr11: 68,233,059-68,759,151 , GRCh37.p13 chr11: 68,000,526-68,526,619 GAL, LOC105369363, 7 more genes
    nsv6912611copy number variation1nstd229human GRCh38 chr11: 68,265,957-68,280,115 , GRCh37.p13 chr11: 68,033,425-68,047,583 LOC105369363, C11orf24
    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
    nsv6461132copy number variation1nstd223human GRCh38 chr11: 68,265,957-68,280,114 , GRCh37.p13 chr11: 68,033,425-68,047,582 LOC105369363, C11orf24
    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
    nsv6285497insertion2nstd214human GRCh38 chr11: 68,264,542-68,264,542 , GRCh37.p13 chr11: 68,032,010-68,032,010 C11orf24
    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
    nsv6086958insertion1nstd212human GRCh38 chr11: 68,264,684-68,264,684 , GRCh37.p13 chr11: 68,032,152-68,032,152 C11orf24
    nsv6080838insertion1nstd212human GRCh38 chr11: 68,264,542-68,264,542 , GRCh37.p13 chr11: 68,032,010-68,032,010 C11orf24
    nsv5968226insertion1nstd209human GRCh38 chr11: 68,264,542-68,264,542 , GRCh37.p13 chr11: 68,032,010-68,032,010 C11orf24
    nsv5650931insertion1nstd207human GRCh38 chr11: 68,264,684-68,264,684 , GRCh37.p13 chr11: 68,032,152-68,032,152 C11orf24
    nsv5645181insertion1nstd207human GRCh38 chr11: 68,264,542-68,264,542 , GRCh37.p13 chr11: 68,032,010-68,032,010 C11orf24
    nsv5553402insertion1nstd206human GRCh38 chr11: 68,264,648-68,264,691 , GRCh37.p13 chr11: 68,032,116-68,032,159 C11orf24
    nsv5546376insertion1nstd206human GRCh38 chr11: 68,264,560-68,264,593 , GRCh37.p13 chr11: 68,032,028-68,032,061 C11orf24
    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
    nsv5133687mobile element insertion1nstd203human GRCh38 chr11: 68,268,890-68,268,908 , GRCh37.p13 chr11: 68,036,358-68,036,376 C11orf24
    nsv4979971copy number variation1nstd200human GRCh38 chr11: 68,265,957-68,280,114 , GRCh37.p13 chr11: 68,033,425-68,047,582 C11orf24, LOC105369363
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