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Items: 1 to 20 of 47

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380721copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 1,774,733-1,785,089 , GRCh38.p12 chr11: 1,753,503-1,763,859 CTSD
    nsv7093927copy number variation1nstd102humanPathogenic GRCh37 chr11: 1,785,002-1,785,089 , GRCh38.p12 chr11: 1,763,772-1,763,859 CTSD
    nsv7093246copy number variation1nstd102humanLikely benign GRCh37 chr11: 1,774,957-1,775,020 , GRCh38 chr11: 1,753,727-1,753,790 CTSD
    nsv6314710copy number variation1nstd102humanLikely benign GRCh38 chr11: 1,755,039-1,755,091 , GRCh37 chr11: 1,776,269-1,776,321 CTSD
    nsv3897310copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,774,508-1,785,629 , GRCh38.p12 chr11: 1,753,278-1,764,399 CTSD
    nsv6309041copy number variation2nstd102humanUncertain significance GRCh37 chr11: 1,774,733-1,778,806 , GRCh38.p12 chr11: 1,753,503-1,757,576 CTSD
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 CTSD, SNORA54, 219 more genes
    nsv3922910copy number variation1nstd102humanPathogenic NCBI36 chr11: 1,116,807-3,191,729 , GRCh38 chr11: 1,132,899-3,213,923 , GRCh37 chr11: 1,126,807-3,235,153 CTSD, CARS1-AS1, 69 more genes
    nsv3915600copy number variation1nstd102humanPathogenic GRCh38 chr11: 758,848-1,998,025 , NCBI36 chr11: 748,848-1,975,831 , GRCh37 chr11: 758,848-2,019,255 CTSD, KRTAP5-5, 58 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 CTSD, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 CTSD, RTN3, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 CTSD, IGHMBP2, 2829 more genes
    nsv3898926copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990 CTSD, OR51L1, 771 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 CTSD, BGLT3, 723 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 CTSD, PCNAP4, 688 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 CTSD, OR52Q1P, 630 more genes
    nsv3894525copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816 CTSD, SDHCP4, 620 more genes
    nsv3912558copy number variation1nstd102humanPathogenic GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865 CTSD, TRIM22, 546 more genes
    nsv3898948copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666 CTSD, MTND5P21, 506 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 CTSD, KRTAP5-3, 457 more genes
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