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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7068895inversion1nstd229human GRCh38 chr11: 100,518,680-109,308,656 , GRCh37.p13 chr11: 100,389,411-109,179,383 LINC02719, RNA5SP349, 121 more genes
    nsv7067245inversion1nstd229human GRCh38 chr11: 103,215,092-107,313,893 , GRCh37.p13 chr11: 103,085,821-107,184,619 DYNC2H1, LINC02719, 51 more genes
    nsv7064393inversion1nstd229human GRCh38 chr11: 105,002,978-105,087,672 , GRCh37.p13 chr11: 104,873,705-104,958,399 CASP1, CARD16, 4 more genes
    nsv7061741inversion1nstd229human GRCh38 chr11: 100,793,881-105,425,000 , GRCh37.p13 chr11: 100,664,612-105,295,727 MTND1P36, LOC102723862, 75 more genes
    nsv6917253copy number variation1nstd229human GRCh38 chr11: 104,925,274-105,041,932 , GRCh37.p13 chr11: 104,796,001-104,912,659 CARD16, CASP5, 2 more genes
    nsv6914639copy number variation1nstd229human GRCh38 chr11: 105,024,553-105,024,646 , GRCh37.p13 chr11: 104,895,280-104,895,373 CASP1
    nsv6913762copy number variation1nstd229human GRCh38 chr11: 104,965,801-105,479,100 , GRCh37.p13 chr11: 104,836,528-105,349,827 CASP1P1, LOC105369469, 11 more genes
    nsv6910913copy number variation1nstd229human GRCh38 chr11: 105,020,790-105,413,477 , GRCh37.p13 chr11: 104,891,517-105,284,204 CASP1, CARD18, 10 more genes
    nsv6908284copy number variation1nstd229human GRCh38 chr11: 105,020,301-105,078,100 , GRCh37.p13 chr11: 104,891,028-104,948,827 LOC107984381, CASP1, 3 more genes
    nsv6907676copy number variation1nstd229human GRCh38 chr11: 104,112,085-107,043,966 , GRCh37.p13 chr11: 103,982,813-106,914,692 GUCY1A2, LINC02719, 36 more genes
    nsv6902953copy number variation1nstd229human GRCh38 chr11: 105,033,644-105,035,181 , GRCh37.p13 chr11: 104,904,371-104,905,908 CASP1
    nsv6901191copy number variation1nstd229human GRCh38 chr11: 105,027,342-105,027,365 , GRCh37.p13 chr11: 104,898,069-104,898,092 CASP1
    nsv6899240copy number variation1nstd229human GRCh38 chr11: 104,320,610-105,453,287 , GRCh37.p13 chr11: 104,191,338-105,324,014 CASP1P2, CASP1P3, 17 more genes
    nsv6637687copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793 GRIA4, MTND1P36, 111 more genes
    nsv6637222copy number variation1nstd102humanUncertain significance GRCh37 chr11: 104,411,149-105,195,575 , GRCh38.p12 chr11: 104,540,421-105,324,848 LOC105369466, CASP4, 16 more genes
    nsv6620944copy number variation1nstd224human GRCh37 chr11: 104,872,823-104,916,018 , GRCh38.p12 chr11: 105,002,096-105,045,291 CASP5, CASP1, 1 more genes
    nsv6620943copy number variation1nstd224human GRCh37 chr11: 104,815,575-105,054,557 , GRCh38.p12 chr11: 104,944,848-105,183,830 CASP5, LOC107984381, 9 more genes
    nsv6578547inversion1nstd223human GRCh38 chr11: 104,070,004-110,020,477 , GRCh37.p13 chr11: 103,940,732-109,891,203 ACAT1, RNU6-654P, 69 more genes
    nsv6475395copy number variation1nstd223human GRCh38 chr11: 104,163,006-105,424,222 , GRCh37.p13 chr11: 104,033,734-105,294,949 OR2AL1P, LOC107984380, 19 more genes
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