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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5721528mobile element insertion2nstd211human GRCh38 chr13: 41,468,941-41,468,941 , GRCh37.p13 chr13: 42,043,077-42,043,077 RGCC
    nsv5704200mobile element insertion2nstd211human GRCh38 chr13: 41,467,968-41,467,968 , GRCh37.p13 chr13: 42,042,104-42,042,104 RGCC
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5563298mobile element insertion1nstd206human GRCh38 chr13: 41,468,941-41,468,992 , GRCh37.p13 chr13: 42,043,077-42,043,128 RGCC
    nsv5423081mobile element insertion1nstd206human GRCh38 chr13: 41,467,968-41,468,010 , GRCh37.p13 chr13: 42,042,104-42,042,146 RGCC
    nsv5199017mobile element insertion1nstd203human GRCh38 chr13: 41,467,585-41,467,604 , GRCh37.p13 chr13: 42,041,721-42,041,740 RGCC
    nsv4618419copy number variation2nstd183human GRCh37 chr13: 42,004,040-42,697,792 , GRCh38.p12 chr13: 41,429,904-42,123,656 KARS1P1, VWA8, 14 more genes
    nsv4602264copy number variation1nstd183human GRCh37 chr13: 40,306,065-46,460,742 , GRCh38.p12 chr13: 39,731,928-45,886,607 , RN7SKP2, 127 more genes
    nsv4530774copy number variation1nstd166human GRCh37.p13 chr13: 42,014,795-42,061,990 , GRCh38.p12 chr13: 41,440,659-41,487,854 RGCC, OR7E37P, 1 more genes
    nsv4508718mobile element insertion1nstd166human GRCh37.p13 chr13: 42,042,088-42,042,088 , GRCh38.p12 chr13: 41,467,952-41,467,952 RGCC
    nsv4387162copy number variation1nstd173human GRCh37 chr13: 41,993,343-42,030,604 , GRCh38.p12 chr13: 41,419,207-41,456,468 OR7E36P, OR7E37P, 2 more genes
    nsv4225948copy number variation1nstd166human GRCh37.p13 chr13: 42,015,950-42,030,000 , GRCh38.p12 chr13: 41,441,814-41,455,864 OR7E37P, RGCC
    nsv3958353insertion1nstd168human GRCh38 chr13: 41,423,080-41,466,897 , GRCh37.p13 chr13: 41,997,216-42,041,033 OR7E36P, RGCC, 2 more genes
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
    nsv3924052copy number variation1nstd102humanPathogenic GRCh38 chr13: 41,288,493-85,137,552 , NCBI36 chr13: 40,760,629-84,609,688 , GRCh37 chr13: 41,862,629-85,711,687 TMEM272, LOC105370241, 535 more genes
    nsv3923911copy number variation1nstd102humanPathogenic GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921 MLNR, SIAH3, 422 more genes
    nsv3923636copy number variation1nstd102humanPathogenic NCBI36 chr13: 37,986,314-50,897,351 , GRCh37 chr13: 39,088,314-51,999,350 , GRCh38 chr13: 38,514,177-51,425,214 TUSC8, SNORA31B, 251 more genes
    nsv3922463copy number variation1nstd102humanPathogenic NCBI36 chr13: 18,418,322-114,088,205 , GRCh37 chr13: 19,520,322-115,070,103 , GRCh38 chr13: 18,946,182-114,304,628 TULP3P1, LOC105370349, 1311 more genes
    nsv3921404copy number variation1nstd102humanPathogenic GRCh37 chr13: 31,592,297-49,065,340 , GRCh38 chr13: 31,018,160-48,491,204 , NCBI36 chr13: 30,490,297-47,963,341 MIR8079, ZDHHC4P1, 280 more genes
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