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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
    nsv6916063copy number variation1nstd229human GRCh38 chr11: 7,509,002-7,512,072 , GRCh37.p13 chr11: 7,530,233-7,533,303 PPFIBP2, OLFML1
    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
    nsv6909945copy number variation1nstd229human GRCh38 chr11: 7,491,543-7,491,765 , GRCh37.p13 chr11: 7,512,774-7,512,996 OLFML1
    nsv6909834copy number variation1nstd229human GRCh38 chr11: 7,500,410-7,506,991 , GRCh37.p13 chr11: 7,521,641-7,528,222 OLFML1
    nsv6908482copy number variation1nstd229human GRCh38 chr11: 7,485,701-7,493,900 , GRCh37.p13 chr11: 7,506,932-7,515,131 OLFML1
    nsv6908258copy number variation1nstd229human GRCh38 chr11: 7,504,942-7,507,309 , GRCh37.p13 chr11: 7,526,173-7,528,540 OLFML1
    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
    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
    nsv6585747inversion1nstd223human GRCh38 chr11: 7,504,998-7,505,560 , GRCh37.p13 chr11: 7,526,229-7,526,791 OLFML1
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6449808copy number variation1nstd223human GRCh38 chr11: 7,491,543-7,491,765 , GRCh37.p13 chr11: 7,512,774-7,512,996 OLFML1
    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
    nsv6313977copy number variation1nstd102humanUncertain significance GRCh37 chr11: 7,502,249-7,570,109 , GRCh38.p12 chr11: 7,481,018-7,548,878 OLFML1, PPFIBP2
    nsv6247737mobile element insertion1nstd215human GRCh38 chr11: 7,501,761-7,501,761 , GRCh37.p13 chr11: 7,522,992-7,522,992 OLFML1
    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
    nsv6086528insertion1nstd212human GRCh38 chr11: 7,491,628-7,491,628 , GRCh37.p13 chr11: 7,512,859-7,512,859 OLFML1
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