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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148239copy number variation1nstd102humanPathogenic GRCh38 chr13: 98,343,655-110,990,677 , GRCh37.p13 chr13: 98,995,909-111,643,024 CLYBL-AS3, PPIAP24, 162 more genes
    nsv7075726inversion1nstd229human GRCh38 chr13: 103,367,726-104,921,977 , GRCh37.p13 chr13: 104,020,076-105,574,328 LINC01309, RPL7P45, 8 more genes
    nsv7072238inversion1nstd229human GRCh38 chr13: 103,363,903-104,918,685 , GRCh37.p13 chr13: 104,016,253-105,571,036 RPL7P45, LOC105370340, 8 more genes
    nsv7069455inversion1nstd229human GRCh38 chr13: 104,397,285-105,386,238 , GRCh37.p13 chr13: 105,049,635-106,038,588 LOC105370343, LOC107984608, 6 more genes
    nsv7065956inversion1nstd229human GRCh38 chr13: 103,464,522-105,138,770 , GRCh37.p13 chr13: 104,116,872-105,791,121 RPL7P45, LOC107984606, 7 more genes
    nsv7059684inversion1nstd229human GRCh38 chr13: 104,830,831-104,830,906 , GRCh37.p13 chr13: 105,483,182-105,483,257 LOC107984607, LOC107984606
    nsv6952873copy number variation1nstd229human GRCh38 chr13: 104,825,788-104,829,267 , GRCh37.p13 chr13: 105,478,139-105,481,618 LOC107984607, LOC107984606
    nsv6939159copy number variation1nstd229human GRCh38 chr13: 104,814,124-104,821,492 , GRCh37.p13 chr13: 105,466,475-105,473,843 RPL7P45, LOC107984607, 1 more genes
    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
    nsv6637615copy number variation1nstd102humanPathogenic GRCh37 chr13: 93,535,335-105,788,229 , GRCh38.p12 chr13: 92,883,082-105,135,878 SNORD13G, FTLP8, 162 more genes
    nsv6637531copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,334,135-110,383,902 , GRCh38.p12 chr13: 99,681,881-109,731,555 ARGLU1, LINC00343, 101 more genes
    nsv6637400copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258 LOC107984609, LINC00354, 265 more genes
    nsv6637217copy number variation1nstd102humanPathogenic GRCh37 chr13: 99,421,603-115,107,733 , GRCh38.p12 chr13: 98,769,349-114,342,258 LOC107984609, CLYBL-AS2, 231 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
    nsv6622100copy number variation1nstd224human GRCh37 chr13: 105,464,837-105,716,018 , GRCh38.p12 chr13: 104,812,486-105,063,667 RPL7P45, LOC105370342, 5 more genes
    nsv6481840copy number variation1nstd223human GRCh38 chr13: 104,825,788-104,829,263 , GRCh37.p13 chr13: 105,478,139-105,481,614 LOC107984606, LOC107984607
    nsv6315552copy number variation1nstd102humanPathogenic GRCh37 chr13: 89,490,345-115,062,235 , GRCh38.p12 chr13: 88,838,091-114,296,760 MIR20A, MIR548AR, 347 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
    nsv6314066copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,258,328-115,107,733 , GRCh38.p12 chr13: 99,606,074-114,342,258 MIR4502, GRTP1-AS1, 208 more genes
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