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Items: 1 to 20 of 71

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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
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv6915733copy number variation1nstd229human GRCh38 chr11: 68,747,301-69,325,100 , GRCh37.p13 chr11: 68,514,769-69,139,868 MRPL21, MRGPRF, 15 more genes
    nsv6910375copy number variation1nstd229human GRCh38 chr11: 68,978,425-68,984,019 , GRCh37.p13 chr11: 68,745,894-68,751,487 MRGPRD
    nsv6907420copy number variation1nstd229human GRCh38 chr11: 68,667,001-69,103,200 , GRCh37.p13 chr11: 68,434,469-68,870,668 TPCN2, CPT1A, 10 more genes
    nsv6906293copy number variation1nstd229human GRCh38 chr11: 68,644,601-69,077,300 , GRCh37.p13 chr11: 68,412,069-68,844,768 MRGPRD, IGHMBP2, 9 more genes
    nsv6902124copy number variation1nstd229human GRCh38 chr11: 68,967,083-68,987,220 , GRCh37.p13 chr11: 68,734,552-68,754,688 MRGPRD
    nsv6474873copy number variation1nstd223human GRCh38 chr11: 68,967,083-68,987,217 , GRCh37.p13 chr11: 68,734,552-68,754,685 MRGPRD
    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
    nsv6132374copy number variation1nstd213human GRCh37 chr11: 68,610,000-69,350,001 , GRCh38.p12 chr11: 68,842,532-69,535,233 TPCN2, IFITM9P, 18 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
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4715326copy number variation1nstd195human GRCh37 chr11: 68,355,451-69,089,801 , GRCh38.p12 chr11: 68,587,983-69,322,333 , CPT1A, 19 more genes
    nsv4712792copy number variation1nstd195human GRCh37 chr11: 68,629,801-69,089,801 , GRCh38.p12 chr11: 68,862,333-69,322,333 , LOC338694, 14 more genes
    nsv4528628copy number variation1nstd166human GRCh37.p13 chr11: 68,306,151-68,837,546 , GRCh38.p12 chr11: 68,538,683-69,070,078 GAL, LOC107984343, 10 more genes
    nsv4202648copy number variation1nstd166human GRCh37.p13 chr11: 68,745,894-68,751,483 , GRCh38.p12 chr11: 68,978,425-68,984,015 MRGPRD
    nsv3920906copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 66,741,311-68,972,547 , GRCh37 chr11: 66,984,735-69,263,366 , GRCh38 chr11: 67,217,264-69,448,598 GRK2, ALDH3B1, 82 more genes
    nsv3917463copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 67,555,736-70,982,189 , GRCh37 chr11: 67,799,160-71,304,541 , GRCh38 chr11: 68,031,693-71,593,495 CCND1, CHKA, 71 more genes
    nsv3914930copy number variation1nstd102humanLikely benign GRCh37 chr11: 67,973,430-69,395,243 , GRCh38 chr11: 68,205,963-69,580,475 , NCBI36 chr11: 67,730,006-69,104,424 LINC02747, LOC105369366, 27 more genes
    nsv3909768copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 67,799,160-70,701,268 , GRCh38.p12 chr11: 68,031,693-70,855,163 CCND1, CHKA, 56 more genes
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