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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980384copy number variation1nstd102humanLikely benign GRCh38 chr11: 2,884,905-2,885,036 , GRCh37 chr11: 2,906,135-2,906,266 CDKN1C
    nsv5980375copy number variation1nstd102humanLikely benign GRCh37 chr11: 2,906,091-2,906,168 , GRCh38 chr11: 2,884,861-2,884,938 CDKN1C
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5674258delins1nstd102humanLikely benign GRCh37 chr11: 2,906,099-2,906,100 , GRCh38 chr11: 2,884,869-2,884,870 CDKN1C
    nsv5672612copy number variation1nstd102humanLikely benign GRCh38 chr11: 2,884,954-2,885,025 , GRCh37 chr11: 2,906,184-2,906,255 CDKN1C
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5373392translocation1nstd200human GRCh38 chr11: 2,884,841-2,884,841 , GRCh38 chrX: 154,390,485-154,390,485 , GRCh37.p13 chrX|NW_003871103.3: 1,824,464-1,824,464 , GRCh37.p13 chrX: 153,618,845-153,618,845 , GRCh37.p13 chr11: 2,906,071-2,906,071 CDKN1C
    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
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4728919copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,629,917-2,902,668 , GRCh38.p12 chr11: 2,608,687-2,881,438 KCNQ1-AS1, KCNQ1, 4 more genes
    nsv4683295copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,905,209-2,906,985 , GRCh38.p12 chr11: 2,883,979-2,885,755 , GRCh38.p12 chr11|NT_187585.1: 116,158-117,965 SLC22A18AS, CDKN1C, 1 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
    nsv4679705copy number variation1nstd189human GRCh37.p13 chr11: 2,339,823-3,832,257 , GRCh38.p12 chr11: 2,318,593-3,811,027 , ART1, 50 more genes
    nsv4675579copy number variation1nstd102humanUncertain significance GRCh37 chr11: 2,683,937-3,207,439 , GRCh38.p12 chr11|NT_187585.1: 1-296,883 , GRCh38.p12 chr11: 2,662,707-3,186,209 CDKN1C, KCNQ1DN, 15 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
    nsv4206796copy number variation1nstd166human GRCh37.p13 chr11: 2,903,277-2,903,348 , GRCh38.p12 chr11|NT_187585.1: 114,227-114,298 , GRCh38.p12 chr11: 2,882,047-2,882,118 CDKN1C
    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
    nsv3924397copy number variation1nstd102humanconflicting data from submitters NCBI36 chr11: 2,861,520-2,861,618 , GRCh37 chr11: 2,904,944-2,905,042 , GRCh38 chr11: 2,883,714-2,883,812 CDKN1C
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