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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv6915986copy number variation1nstd229human GRCh38 chr11: 64,935,377-65,143,014 , GRCh37.p13 chr11: 64,702,849-64,910,485 TM7SF2, HIGD1AP10, 19 more genes
    nsv6906511copy number variation1nstd229human GRCh38 chr11: 65,030,362-65,030,510 , GRCh37.p13 chr11: 64,797,834-64,797,982 ARL2-SNX15, SNX15
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6594994inversion1nstd223human GRCh38 chr11: 65,033,715-65,034,212 , GRCh37.p13 chr11: 64,801,187-64,801,684 ARL2-SNX15, SNX15
    nsv6576465inversion1nstd223human GRCh38 chr11: 65,028,812-65,029,285 , GRCh37.p13 chr11: 64,796,284-64,796,757 ARL2-SNX15, SNX15
    nsv6470631copy number variation1nstd223human GRCh38 chr11: 64,935,377-65,143,014 , GRCh37.p13 chr11: 64,702,849-64,910,485 MAJIN, HIGD1AP10, 19 more genes
    nsv6461693copy number variation1nstd223human GRCh38 chr11: 65,028,970-65,030,242 , GRCh37.p13 chr11: 64,796,442-64,797,714 SNX15, ARL2-SNX15
    nsv6458120copy number variation1nstd223human GRCh38 chr11: 65,040,220-65,093,556 , GRCh37.p13 chr11: 64,807,692-64,861,028 ZFPL1, NAALADL1, 5 more genes
    nsv6457728copy number variation1nstd223human GRCh38 chr11: 65,036,707-65,039,037 , GRCh37.p13 chr11: 64,804,179-64,806,509 SNX15, ARL2-SNX15, 1 more genes
    nsv6456968copy number variation1nstd223human GRCh38 chr11: 65,029,729-65,030,687 , GRCh37.p13 chr11: 64,797,201-64,798,159 SNX15, ARL2-SNX15
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6142989copy number variation1nstd206human GRCh38 chr11: 65,023,467-65,036,959 , GRCh37.p13 chr11: 64,790,939-64,804,431 SNX15, ARL2-SNX15, 1 more genes
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5979747insertion1nstd209human GRCh37.p13 chr11: 64,806,501-64,806,501 , GRCh38 chr11: 65,039,029-65,039,029 SAC3D1, SNX15, 1 more genes
    nsv5973609insertion1nstd209human GRCh37.p13 chr11: 64,793,251-64,793,251 , GRCh38 chr11: 65,025,779-65,025,779 SNX15, ARL2-SNX15, 1 more genes
    nsv5383722mobile element deletion1nstd186human GRCh37 chr11: 64,797,841-64,797,982 , GRCh38.p12 chr11: 65,030,369-65,030,510 ARL2-SNX15, SNX15
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