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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
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv7059680inversion1nstd229human GRCh38 chr11: 71,462,823-71,462,954 , GRCh37.p13 chr11: 71,173,869-71,174,000 NADSYN1
    nsv6913831copy number variation1nstd229human GRCh38 chr11: 71,448,477-71,504,388 , GRCh37.p13 chr11: 71,159,523-71,215,434 MIR6754, NADSYN1, 2 more genes
    nsv6912073copy number variation1nstd229human GRCh38 chr11: 71,501,700-71,504,678 , GRCh37.p13 chr11: 71,212,746-71,215,724 NADSYN1, S100A11P3
    nsv6908275copy number variation1nstd229human GRCh38 chr11: 71,281,500-72,194,614 , GRCh37.p13 chr11: 71,088,949-71,905,658 DEFB130C, ANAPC15, 40 more genes
    nsv6902947copy number variation1nstd229human GRCh38 chr11: 71,467,500-71,468,678 , GRCh37.p13 chr11: 71,178,546-71,179,724 NADSYN1
    nsv6901984copy number variation1nstd229human GRCh38 chr11: 71,499,753-71,500,061 , GRCh37.p13 chr11: 71,210,799-71,211,107 NADSYN1
    nsv6637237copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,051,703-71,655,505 , GRCh38.p12 chr11: 71,340,657-71,944,459 FAM86C1P, KRTAP5-7, 28 more genes
    nsv6621132copy number variation1nstd224human GRCh37 chr11: 71,152,329-71,167,449 , GRCh38.p12 chr11: 71,441,283-71,456,403 NADSYN1, DHCR7
    nsv6463414copy number variation1nstd223human GRCh38 chr11: 71,501,700-71,504,676 , GRCh37.p13 chr11: 71,212,746-71,215,722 NADSYN1, S100A11P3
    nsv6461624copy number variation1nstd223human GRCh38 chr11: 71,459,054-71,459,458 , GRCh37.p13 chr11: 71,170,100-71,170,504 NADSYN1
    nsv6457258copy number variation1nstd223human GRCh38 chr11: 71,481,081-71,482,306 , GRCh37.p13 chr11: 71,192,127-71,193,352 NADSYN1
    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
    nsv6206922copy number variation1nstd214human GRCh38 chr11: 71,459,051-71,459,110 , GRCh37.p13 chr11: 71,170,097-71,170,156 NADSYN1
    nsv6198802copy number variation1nstd214human GRCh38 chr11: 71,482,428-71,482,500 , GRCh37.p13 chr11: 71,193,474-71,193,546 NADSYN1
    nsv6189169copy number variation1nstd214human GRCh38 chr11: 71,482,609-71,482,680 , GRCh37.p13 chr11: 71,193,655-71,193,726 NADSYN1
    nsv6188063copy number variation1nstd214human GRCh38 chr11: 71,474,711-71,474,782 , GRCh37.p13 chr11: 71,185,757-71,185,828 NADSYN1
    nsv6143563copy number variation1nstd206human GRCh38 chr11: 71,459,016-71,459,217 , GRCh37.p13 chr11: 71,170,062-71,170,263 NADSYN1
    nsv6091264insertion1nstd212human GRCh38 chr11: 71,459,184-71,459,184 , GRCh37.p13 chr11: 71,170,230-71,170,230 NADSYN1
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