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Items: 1 to 20 of 134

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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
    nsv7093933copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 65,325,080-65,639,825 , GRCh38.p12 chr11: 65,557,609-65,872,354 ZNRD2-DT, ZNRD2, 22 more genes
    nsv7062888inversion1nstd229human GRCh38 chr11: 65,331,143-66,048,384 , GRCh37.p13 chr11: 65,098,614-65,815,855 FAUP4, MAP3K11, 50 more genes
    nsv7061449inversion1nstd229human GRCh38 chr11: 65,331,281-66,115,058 , GRCh37.p13 chr11: 65,098,752-65,882,529 LOC100420020, LINC02736, 53 more genes
    nsv6913424copy number variation1nstd229human GRCh38 chr11: 65,646,801-65,653,000 , GRCh37.p13 chr11: 65,414,272-65,420,471 RELA, SIPA1, 1 more genes
    nsv6912389copy number variation1nstd229human GRCh38 chr11: 65,604,598-65,954,847 , GRCh37.p13 chr11: 65,372,069-65,722,318 RNASEH2C, C11orf68, 24 more genes
    nsv6912151copy number variation1nstd229human GRCh38 chr11: 65,642,127-65,646,559 , GRCh37.p13 chr11: 65,409,598-65,414,030 SIPA1
    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
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6899734copy number variation1nstd229human GRCh38 chr11: 65,635,268-65,640,253 , GRCh37.p13 chr11: 65,402,739-65,407,724 MIR4690, PCNX3, 1 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
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 more genes
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 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
    nsv5272481copy number variation1nstd204human GRCh38.p13 chr11: 65,533,701-65,718,000 , GRCh37.p13 chr11: 65,301,172-65,485,471 ZNRD2, ZNRD2-DT, 15 more genes
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv5262374copy number variation1nstd204human GRCh38.p13 chr11: 65,373,701-65,675,900 , GRCh37.p13 chr11: 65,141,172-65,443,371 , MIR612, 23 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
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