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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5513168copy number variation1nstd206human GRCh38 chr11: 88,307,910-88,307,990 , GRCh37.p13 chr11: 88,041,078-88,041,158 CTSC
    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
    nsv5373776translocation1nstd200human GRCh38 chr11: 88,295,940-88,295,940 , GRCh38 chr11: 88,297,157-88,297,157 , GRCh37.p13 chr11: 88,029,108-88,029,108 , GRCh37.p13 chr11: 88,030,325-88,030,325 CTSC
    nsv5305798copy number variation1nstd204human GRCh38.p13 chr11: 88,301,672-88,308,689 , GRCh37.p13 chr11: 88,034,840-88,041,857 CTSC
    nsv5264916copy number variation1nstd204human GRCh38.p13 chr11: 88,301,757-88,308,885 , GRCh37.p13 chr11: 88,034,925-88,042,053 CTSC
    nsv4971468copy number variation1nstd200human GRCh38 chr11: 88,301,679-88,308,685 , GRCh37.p13 chr11: 88,034,847-88,041,853 CTSC
    nsv4971467copy number variation1nstd200human GRCh38 chr11: 88,290,651-88,364,866 , GRCh37.p13 chr11: 88,023,819-88,098,034 CTSC, LOC101929174
    nsv4971421copy number variation1nstd200human GRCh38 chr11: 87,146,136-88,345,646 , GRCh37.p13 chr11: 86,857,178-88,078,814 LOC100420680, PSMA2P1, 11 more genes
    nsv4840034copy number variation1nstd200human GRCh37 chr11: 88,034,847-88,041,853 , GRCh38.p12 chr11: 88,301,679-88,308,685 CTSC
    nsv4832551copy number variation1nstd200human GRCh37 chr11: 88,023,819-88,098,034 , GRCh38.p12 chr11: 88,290,651-88,364,866 LOC101929174, CTSC
    nsv4832360copy number variation1nstd200human GRCh37 chr11: 86,857,178-88,078,814 , GRCh38.p12 chr11: 87,146,136-88,345,646 MTCYBP41, CTSC, 11 more genes
    nsv4681462copy number variation1nstd102humanUncertain significance GRCh37 chr11: 88,027,154-88,070,895 , GRCh38.p12 chr11: 88,293,986-88,337,727 CTSC, LOC101929174
    nsv4675217copy number variation1nstd102humanPathogenic GRCh37 chr11: 84,830,143-92,029,933 , GRCh38.p12 chr11: 85,119,099-92,296,767 LINC02756, FNTAP1, 98 more genes
    nsv4455473copy number variation1nstd102humanPathogenic GRCh37 chr11: 88,023,054-88,100,191 , GRCh38.p12 chr11: 88,289,886-88,367,023 CTSC, LOC101929174
    nsv4334739sequence alteration1nstd166human GRCh37.p13 chr11: 88,028,900-88,030,398 , GRCh38.p12 chr11: 88,295,732-88,297,230 CTSC
    nsv4208175copy number variation1nstd166human GRCh37.p13 chr11: 88,041,078-88,041,158 , GRCh38.p12 chr11: 88,307,910-88,307,990 CTSC
    nsv4207333copy number variation1nstd166human GRCh37.p13 chr11: 84,827,860-92,033,952 , GRCh38.p12 chr11: 85,116,816-92,300,786 , ME3-DT, 101 more genes
    nsv3922508copy number variation1nstd102humanPathogenic GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037 AMOTL1, LNCRNA-IUR, 240 more genes
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 LOC105369441, RNU6-1135P, 296 more genes
    nsv3920613copy number variation1nstd102humanUncertain significance NCBI36 chr11: 87,459,874-87,685,399 , GRCh37.p13 chr11: 87,820,226-88,045,751 , GRCh38.p12 chr11: 88,087,058-88,312,583 CTSC, MIR3166, 1 more genes
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