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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5259948copy number variation1nstd204human GRCh38.p13 chr11: 1,804,001-2,194,300 , GRCh37.p13 chr11: 1,825,231-2,215,530 H19, INS, 20 more genes
    nsv5251619copy number variation1nstd204human GRCh38.p13 chr11: 1,993,101-1,995,100 , GRCh37.p13 chr11: 2,014,331-2,016,330 MRPL23, LINC01219, 2 more genes
    nsv4847422copy number variation1nstd200human GRCh37 chr11: 2,021,908-2,023,979 , GRCh38.p12 chr11: 2,000,678-2,002,749 MRPL23, H19
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4729545copy number variation1nstd102humanPathogenic GRCh37 chr11: 1,436,158-2,321,134 , GRCh38.p12 chr11: 1,414,928-2,299,904 MIR4686, H19, 40 more genes
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4681827copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,616-2,906,985 , GRCh38.p12 chr11: 532,616-2,885,755 LOC105376517, KRTAP5-2, 99 more genes
    nsv4681514copy number variation2nstd102humanUncertain significance GRCh37 chr11: 612,625-2,193,840 , GRCh38.p12 chr11: 612,625-2,172,610 LINC02688, TNNI2, 74 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv3924864copy number variation1nstd102humanUncertain significance GRCh37 chr11: 1,996,741-3,645,369 , NCBI36 chr11: 1,953,317-3,601,945 , GRCh38 chr11: 1,975,511-3,624,139 TSSC2, CD81, 54 more genes
    nsv3923626copy number variation1nstd102humanBenign GRCh37 chr11: 2,016,675-2,016,841 , NCBI36 chr11: 1,973,251-1,973,417 , GRCh38 chr11: 1,995,445-1,995,611 MIR675, H19, 1 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 CARS1-AS1, TH, 69 more genes
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
    nsv3919461copy number variation1nstd102humanPathogenic NCBI36 chr11: 1,515,185-3,338,575 , GRCh38 chr11: 1,537,379-3,360,769 , GRCh37 chr11: 1,558,609-3,381,999 C11orf21, SLC22A18AS, 67 more genes
    nsv3918870copy number variation1nstd102humanPathogenic GRCh38 chr11: 196,855-2,116,185 , NCBI36 chr11: 186,855-2,093,991 , GRCh37 chr11: 196,855-2,137,415 LOC105376506, KRTAP5-4, 99 more genes
    nsv3918376copy number variation1nstd102humanPathogenic NCBI36 chr11: 128,203-5,440,733 , GRCh37.p13 chr11: 138,203-5,484,157 , GRCh38.p12 chr11: 138,203-5,462,927 HBG2, OR51T1, 262 more genes
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