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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076777inversion1nstd229human GRCh38 chr11: 114,180,972-114,778,739 , GRCh37.p13 chr11: 114,051,694-114,649,461 NNMT, NXPE4, 12 more genes
    nsv7064894inversion1nstd229human GRCh38 chr11: 114,542,877-114,618,972 , GRCh37.p13 chr11: 114,413,599-114,489,694 NXPE2, LOC100132172, 2 more genes
    nsv7064323inversion1nstd229human GRCh38 chr11: 114,580,842-114,632,939 , GRCh37.p13 chr11: 114,451,564-114,503,661 NXPE4, NXPE2, 1 more genes
    nsv7060444inversion1nstd229human GRCh38 chr11: 114,035,283-115,207,618 , GRCh37.p13 chr11: 113,906,005-115,078,338 CADM1, LOC105369506, 13 more genes
    nsv6901697copy number variation1nstd229human GRCh38 chr11: 114,594,166-114,596,881 , GRCh37.p13 chr11: 114,464,888-114,467,603 NXPE2, NXPE4
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6620884copy number variation1nstd224human GRCh37 chr11: 114,411,343-114,442,145 , GRCh38.p12 chr11: 114,540,621-114,571,423 NXPE4, NXPE1, 1 more genes
    nsv6579484inversion1nstd223human GRCh38 chr11: 114,039,971-117,481,220 , GRCh37.p13 chr11: 113,910,693-117,351,935 RNF214, LOC107984372, 52 more genes
    nsv6472344copy number variation1nstd223human GRCh38 chr11: 114,585,701-114,592,300 , GRCh37.p13 chr11: 114,456,423-114,463,022 NXPE2, NXPE4
    nsv6462750copy number variation1nstd223human GRCh38 chr11: 114,530,888-114,735,901 , GRCh37.p13 chr11: 114,401,610-114,606,623 LOC100132172, NXPE2, 2 more genes
    nsv6458338copy number variation1nstd223human GRCh38 chr11: 114,573,452-114,573,649 , GRCh37.p13 chr11: 114,444,174-114,444,371 NXPE2, NXPE4
    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
    nsv6303302copy number variation1nstd186human GRCh37 chr11: 114,462,188-114,462,248 , GRCh38.p12 chr11: 114,591,466-114,591,526 NXPE4, NXPE2
    nsv6302509copy number variation1nstd186human GRCh37 chr11: 114,457,846-114,503,520 , GRCh38.p12 chr11: 114,587,124-114,632,798 NXPE4, NXPE2
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6198125copy number variation1nstd214human GRCh38 chr11: 114,576,977-114,577,044 , GRCh37.p13 chr11: 114,447,699-114,447,766 NXPE2, NXPE4
    nsv6197485copy number variation1nstd214human GRCh38 chr11: 114,576,994-114,577,057 , GRCh37.p13 chr11: 114,447,716-114,447,779 NXPE4, NXPE2
    nsv6192515copy number variation1nstd214human GRCh38 chr11: 114,595,931-114,596,009 , GRCh37.p13 chr11: 114,466,653-114,466,731 NXPE4, NXPE2
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