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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6915481copy number variation1nstd229human GRCh38 chr11: 7,014,782-7,919,611 , GRCh37.p13 chr11: 7,036,013-7,941,158 SYT9, OR10AB1P, 20 more genes
    nsv6910288copy number variation1nstd229human GRCh38 chr11: 7,458,712-7,458,808 , GRCh37.p13 chr11: 7,479,943-7,480,039 SYT9, SYT9-AS1
    nsv6907915copy number variation1nstd229human GRCh38 chr11: 7,444,789-7,456,440 , GRCh37.p13 chr11: 7,466,020-7,477,671 SYT9, SYT9-AS1
    nsv6907023copy number variation1nstd229human GRCh38 chr11: 7,452,332-7,452,440 , GRCh37.p13 chr11: 7,473,563-7,473,671 SYT9-AS1, SYT9
    nsv6906971copy number variation1nstd229human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 RIC3, LOC644656, 86 more genes
    nsv6899412copy number variation1nstd229human GRCh38 chr11: 7,452,443-7,461,466 , GRCh37.p13 chr11: 7,473,674-7,482,697 SYT9, SYT9-AS1
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6637245copy number variation1nstd102humanUncertain significance GRCh37 chr11: 7,326,212-7,525,985 , GRCh38.p12 chr11: 7,304,981-7,504,754 SYT9, SYT9-AS1, 1 more genes
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6442855copy number variation1nstd223human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 LOC105369149, C11orf16, 86 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6132276copy number variation1nstd213human GRCh37 chr11: 7,180,000-8,030,001 , GRCh38.p12 chr11: 7,158,769-8,008,454 PPFIBP2, EIF3F, 22 more genes
    nsv6086329insertion1nstd212human GRCh38 chr11: 7,442,720-7,442,720 , GRCh37.p13 chr11: 7,463,951-7,463,951 SYT9-AS1, SYT9
    nsv5184905mobile element insertion1nstd203human GRCh38 chr11: 7,446,298-7,446,315 , GRCh37.p13 chr11: 7,467,529-7,467,546 SYT9-AS1, SYT9
    nsv4978091copy number variation1nstd200human GRCh38 chr11: 7,445,688-7,445,769 , GRCh37.p13 chr11: 7,466,919-7,467,000 SYT9, SYT9-AS1
    nsv4844592copy number variation1nstd200human GRCh37 chr11: 7,458,302-7,458,453 , GRCh38.p12 chr11: 7,437,071-7,437,222 SYT9, SYT9-AS1
    nsv4840839copy number variation1nstd200human GRCh37 chr11: 7,466,919-7,467,000 , GRCh38.p12 chr11: 7,445,688-7,445,769 SYT9, SYT9-AS1
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
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