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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063899inversion1nstd229human GRCh38 chr13: 87,663,888-92,195,406 , GRCh37.p13 chr13: 88,316,143-92,847,659 RNU6-75P, LOC105370311, 50 more genes
    nsv7063565inversion1nstd229human GRCh38 chr13: 85,643,741-87,853,235 , GRCh37.p13 chr13: 86,217,876-88,505,490 LINC00397, MIR4500, 16 more genes
    nsv7062771inversion1nstd229human GRCh38 chr13: 86,949,883-89,810,099 , GRCh37.p13 chr13: 87,602,138-90,462,353 LINC00433, LOC105370302, 25 more genes
    nsv6956057copy number variation1nstd229human GRCh38 chr13: 86,803,289-88,366,933 , GRCh37.p13 chr13: 87,455,544-89,019,188 UBBP5, LOC105370301, 14 more genes
    nsv6954411copy number variation1nstd229human GRCh38 chr13: 87,672,447-87,721,101 , GRCh37.p13 chr13: 88,324,702-88,373,356 LOC112268106, SLITRK5
    nsv6945531copy number variation1nstd229human GRCh38 chr13: 87,667,860-87,671,184 , GRCh37.p13 chr13: 88,320,115-88,323,439 SLITRK5, MIR4500HG
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637507copy number variation1nstd102humanUncertain significance GRCh37 chr13: 86,667,980-91,833,689 , GRCh38.p12 chr13: 86,093,845-91,181,435 LINC00559, LOC105370304, 47 more genes
    nsv6637451copy number variation1nstd102humanUncertain significance GRCh37 chr13: 85,665,879-90,460,716 , GRCh38.p12 chr13: 85,091,744-89,808,462 LINC00373, LINC00375, 37 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6486171copy number variation1nstd223human GRCh38 chr13: 87,677,201-87,678,000 , GRCh37.p13 chr13: 88,329,456-88,330,255 SLITRK5
    nsv6485253copy number variation1nstd223human GRCh38 chr13: 86,803,287-88,366,930 , GRCh37.p13 chr13: 87,455,542-89,019,185 UBBP5, RPL29P29, 14 more genes
    nsv6484471copy number variation1nstd223human GRCh38 chr13: 87,651,601-87,701,600 , GRCh37.p13 chr13: 88,303,856-88,353,855 SLITRK5, MIR4500HG, 1 more genes
    nsv6478135copy number variation1nstd223human GRCh38 chr13: 87,655,201-87,701,600 , GRCh37.p13 chr13: 88,307,456-88,353,855 LOC112268106, MIR4500HG, 1 more genes
    nsv6477893copy number variation1nstd223human GRCh38 chr13: 87,668,701-87,687,800 , GRCh37.p13 chr13: 88,320,956-88,340,055 LOC112268106, MIR4500HG, 1 more genes
    nsv6476340copy number variation1nstd223human GRCh38 chr13: 87,640,101-87,705,000 , GRCh37.p13 chr13: 88,292,356-88,357,255 LOC112268106, MIR4500HG, 1 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314171copy number variation1nstd102humanPathogenic GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258 MIR4705, LOC102724149, 430 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6313971copy number variation1nstd102humanPathogenic GRCh37 chr13: 85,037,147-115,107,733 , GRCh38.p12 chr13: 84,463,012-114,342,258 BRK1P2, UGGT2, 386 more genes
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