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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7062888inversion1nstd229human GRCh38 chr11: 65,331,143-66,048,384 , GRCh37.p13 chr11: 65,098,614-65,815,855 FAUP4, MAP3K11, 50 more genes
    nsv7061449inversion1nstd229human GRCh38 chr11: 65,331,281-66,115,058 , GRCh37.p13 chr11: 65,098,752-65,882,529 LOC100420020, LINC02736, 53 more genes
    nsv6915026copy number variation1nstd229human GRCh38 chr11: 65,462,801-65,529,700 , GRCh37.p13 chr11: 65,230,272-65,297,171 MASCRNA, SNRPGP19, 5 more genes
    nsv6911272copy number variation1nstd229human GRCh38 chr11: 65,494,601-65,500,500 , GRCh37.p13 chr11: 65,262,072-65,267,971 TALAM1, MALAT1
    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
    nsv6905388copy number variation1nstd229human GRCh38 chr11: 65,507,055-65,514,852 , GRCh37.p13 chr11: 65,274,526-65,282,323 SNRPGP19, TALAM1
    nsv6903676copy number variation1nstd229human GRCh38 chr11: 65,496,824-65,500,896 , GRCh37.p13 chr11: 65,264,295-65,268,367 MALAT1, TALAM1
    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
    nsv6464704copy number variation1nstd223human GRCh38 chr11: 65,496,823-65,500,895 , GRCh37.p13 chr11: 65,264,294-65,268,366 MALAT1, TALAM1
    nsv6459254copy number variation1nstd223human GRCh38 chr11: 65,507,601-65,514,200 , GRCh37.p13 chr11: 65,275,072-65,281,671 TALAM1, SNRPGP19
    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
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 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
    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
    nsv5700271mobile element insertion2nstd211human GRCh38 chr11: 65,498,232-65,498,232 , GRCh37.p13 chr11: 65,265,703-65,265,703 MALAT1, TALAM1
    nsv5671123inversion1nstd207human GRCh37.p13 chr11: 65,267,729-65,273,464 , GRCh38 chr11: 65,500,258-65,505,993 MALAT1, MASCRNA, 1 more genes
    nsv5404116mobile element insertion1nstd206human GRCh38 chr11: 65,498,232-65,498,283 , GRCh37.p13 chr11: 65,265,703-65,265,754 TALAM1, MALAT1
    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
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