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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148121copy number variation1nstd102humanPathogenic GRCh37 chr10: 46,284,269-51,870,080 , GRCh38.p12 chr10: 45,788,821-50,110,320 LOC100420617, ZNF488, 108 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7098865copy number variation1nstd102humanLikely pathogenic GRCh37.p13 chr10|NW_003871068.1: 1-2,281,126 , GRCh38 chr10: 45,704,708-50,015,268 , GRCh37.p13 chr10: 46,200,156-51,028,871 CHAT, CTSLP2, 107 more genes
    nsv7093389copy number variation1nstd102humanUncertain significance GRCh37 chr10: 46,584,432-51,974,628 , GRCh38.p12 chr10: 45,931,517-50,214,868 NCOA4, AGAP7P, 106 more genes
    nsv7069878inversion1nstd229human GRCh38 chr10: 47,497,713-51,210,711 , GRCh37.p13 chr10: 46,591,857-52,970,471 MIR4294, SLC18A3, 76 more genes
    nsv7066519inversion1nstd229human GRCh38 chr10: 45,802,941-50,026,843 , GRCh37.p13 chr10|NW_003871068.1: 74,056-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,028,871 RNA5SP317, AHCYP1, 106 more genes
    nsv7060309inversion1nstd229human GRCh38 chr10: 46,173,677-55,799,586 , GRCh37.p13 chr10: 46,591,857-57,559,346 NPY4R, LOC102724603, 138 more genes
    nsv6895769copy number variation1nstd229human GRCh38 chr10: 45,735,504-50,076,220 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 6,619-2,281,126 BMS1P1, AGAP9, 108 more genes
    nsv6894885copy number variation1nstd229human GRCh38 chr10: 49,365,761-49,365,819 , GRCh37.p13 chr10: 50,573,806-50,573,864 DRGX
    nsv6893251copy number variation1nstd229human GRCh38 chr10: 49,394,801-49,396,200 , GRCh37.p13 chr10: 50,602,847-50,604,246 DRGX
    nsv6892093copy number variation1nstd229human GRCh38 chr10: 49,339,401-49,372,300 , GRCh37.p13 chr10: 50,547,446-50,580,346 DRGX
    nsv6887381copy number variation1nstd229human GRCh38 chr10: 49,355,224-49,390,007 , GRCh37.p13 chr10: 50,563,269-50,598,053 DRGX
    nsv6886895copy number variation1nstd229human GRCh38 chr10: 49,370,825-49,374,328 , GRCh37.p13 chr10: 50,578,870-50,582,374 DRGX
    nsv6886834copy number variation1nstd229human GRCh38 chr10: 45,568,878-51,464,891 , GRCh37.p13 chr10: 46,064,326-53,224,651 PGBD3, MAPK8, 134 more genes
    nsv6885471copy number variation1nstd229human GRCh38 chr10: 48,691,383-50,476,716 , GRCh37.p13 chr10: 49,899,428-52,236,476 SLC18A3, LOC105378298, 35 more genes
    nsv6884472copy number variation1nstd229human GRCh38 chr10: 49,373,825-49,380,972 , GRCh37.p13 chr10: 50,581,871-50,589,018 DRGX
    nsv6881604copy number variation1nstd229human GRCh38 chr10: 49,357,491-49,381,581 , GRCh37.p13 chr10: 50,565,536-50,589,627 DRGX
    nsv6880357copy number variation1nstd229human GRCh38 chr10: 49,370,716-49,378,931 , GRCh37.p13 chr10: 50,578,761-50,586,977 DRGX
    nsv6879005copy number variation1nstd229human GRCh38 chr10: 49,372,315-49,372,486 , GRCh37.p13 chr10: 50,580,361-50,580,532 DRGX
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