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Items: 1 to 20 of 86

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144897insertion1nstd232human GRCh37.p13 chr11: 64,949,652-64,949,652 , GRCh38.p12 chr11: 65,182,181-65,182,181 CAPN1, CAPN1-AS1
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv6913380copy number variation1nstd229human GRCh38 chr11: 65,179,576-65,180,140 , GRCh37.p13 chr11: 64,947,047-64,947,611 CAPN1, CAPN1-AS1
    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
    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
    nsv6289307insertion1nstd214human GRCh38 chr11: 65,182,226-65,182,226 , GRCh37.p13 chr11: 64,949,697-64,949,697 CAPN1-AS1, CAPN1
    nsv6285993insertion1nstd214human GRCh38 chr11: 65,182,181-65,182,181 , GRCh37.p13 chr11: 64,949,652-64,949,652 CAPN1, CAPN1-AS1
    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
    nsv6100351insertion1nstd212human GRCh38 chr11: 65,182,203-65,182,203 , GRCh37.p13 chr11: 64,949,674-64,949,674 CAPN1-AS1, CAPN1
    nsv5921796copy number variation1nstd209human GRCh38 chr11: 65,178,677-65,187,446 , GRCh37.p13 chr11: 64,946,148-64,954,917 CAPN1-AS1, CAPN1
    nsv5917933copy number variation1nstd209human GRCh38 chr11: 65,180,143-65,180,240 , GRCh37.p13 chr11: 64,947,614-64,947,711 CAPN1-AS1, CAPN1
    nsv5851573copy number variation1nstd209human GRCh38 chr11: 65,178,674-65,185,367 , GRCh37.p13 chr11: 64,946,145-64,952,838 CAPN1-AS1, CAPN1
    nsv5648687insertion1nstd207human GRCh38 chr11: 65,182,181-65,182,181 , GRCh37.p13 chr11: 64,949,652-64,949,652 CAPN1, CAPN1-AS1
    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
    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
    nsv4763185insertion1nstd199human GRCh37 chr11: 64,949,668-64,949,668 , GRCh38.p12 chr11: 65,182,197-65,182,197 CAPN1, CAPN1-AS1
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