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Items: 1 to 20 of 120

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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
    nsv7093406copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,178,392-66,433,436 , GRCh38.p12 chr11: 66,410,921-66,665,965 MRPL11, NPAS4, 15 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
    nsv6903953copy number variation1nstd229human GRCh38 chr11: 66,612,180-66,614,712 , GRCh37.p13 chr11: 66,379,651-66,382,183 RNU4-39P, RBM14-RBM4, 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
    nsv6314012copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,188,172-66,402,747 , GRCh38.p12 chr11: 66,420,701-66,635,276 LOC100505524, ZDHHC24, 13 more genes
    nsv6290938copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,963,737-66,581,485 , GRCh38.p12 chr11: 66,196,266-66,814,014 CCS, RN7SL12P, 38 more genes
    nsv6132113copy number variation1nstd213human GRCh37 chr11: 66,380,000-66,540,001 , GRCh38.p12 chr11: 66,612,529-66,772,530 RBM14, RBM4B, 8 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
    nsv6040296copy number variation1nstd212human GRCh38 chr11: 66,614,703-66,615,172 , GRCh37.p13 chr11: 66,382,174-66,382,643 RBM14, RBM14-RBM4, 1 more genes
    nsv5979044insertion1nstd209human GRCh38 chr11: 66,615,753-66,615,753 , GRCh37.p13 chr11: 66,383,224-66,383,224 RBM14, RBM14-RBM4
    nsv5709536mobile element insertion1nstd211human GRCh38 chr11: 66,626,058-66,626,058 , GRCh37.p13 chr11: 66,393,529-66,393,529 RBM14-RBM4, RBM14
    nsv5662700insertion1nstd207human GRCh38 chr11: 66,615,753-66,615,753 , GRCh37.p13 chr11: 66,383,224-66,383,224 RBM14-RBM4, RBM14
    nsv5547304insertion1nstd206human GRCh38 chr11: 66,630,302-66,630,336 , GRCh37.p13 chr11: 66,397,773-66,397,807 RBM14, RBM14-RBM4
    nsv5545046insertion1nstd206human GRCh38 chr11: 66,615,769-66,615,788 , GRCh37.p13 chr11: 66,383,240-66,383,259 RBM14, RBM14-RBM4
    nsv5497035copy number variation1nstd206human GRCh38 chr11: 66,616,500-66,625,074 , GRCh37.p13 chr11: 66,383,971-66,392,545 RBM14, RBM14-RBM4
    nsv5402653mobile element insertion1nstd206human GRCh38 chr11: 66,626,058-66,626,109 , GRCh37.p13 chr11: 66,393,529-66,393,580 RBM14, RBM14-RBM4
    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
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
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