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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094095copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,306,779-65,307,119 , GRCh38.p12 chr11: 65,539,308-65,539,648 LTBP3
    nsv7094094copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,303,404-65,311,040 , GRCh38.p12 chr11: 65,535,933-65,543,569 LTBP3, SCYL1
    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
    nsv7093933copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 65,325,080-65,639,825 , GRCh38.p12 chr11: 65,557,609-65,872,354 ZNRD2-DT, ZNRD2, 22 more genes
    nsv7093932copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,306,531-65,325,450 , GRCh38.p12 chr11: 65,539,060-65,557,979 LTBP3, SCYL1
    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
    nsv6916034copy number variation1nstd229human GRCh38 chr11: 65,535,471-65,544,131 , GRCh37.p13 chr11: 65,302,942-65,311,602 SCYL1, LTBP3
    nsv6915477copy number variation1nstd229human GRCh38 chr11: 65,518,042-65,544,549 , GRCh37.p13 chr11: 65,285,513-65,312,020 LTBP3, SCYL1
    nsv6908039copy number variation1nstd229human GRCh38 chr11: 65,534,579-65,538,828 , GRCh37.p13 chr11: 65,302,050-65,306,299 SCYL1, LTBP3
    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
    nsv6469855copy number variation1nstd223human GRCh38 chr11: 65,518,042-65,544,547 , GRCh37.p13 chr11: 65,285,513-65,312,018 SCYL1, LTBP3
    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
    nsv6303000copy number variation1nstd186human GRCh37 chr11: 65,312,624-65,312,731 , GRCh38.p12 chr11: 65,545,153-65,545,260 LTBP3
    nsv6235842insertion2nstd214human GRCh38 chr11: 65,540,715-65,540,715 , GRCh37.p13 chr11: 65,308,186-65,308,186 LTBP3
    nsv6229559insertion1nstd214human GRCh38 chr11: 65,540,703-65,540,703 , GRCh37.p13 chr11: 65,308,174-65,308,174 LTBP3
    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
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