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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071638inversion1nstd229human GRCh38 chr13: 55,583,879-63,209,085 , GRCh37.p13 chr13: 56,158,014-63,783,218 MIR3169, PCDH20, 66 more genes
    nsv7063310inversion1nstd229human GRCh38 chr13: 60,352,407-63,352,731 , GRCh37.p13 chr13: 60,926,541-63,926,864 TDRD3, LOC105370230, 23 more genes
    nsv7059850inversion1nstd229human GRCh38 chr13: 61,334,865-61,626,594 , GRCh37.p13 chr13: 61,908,998-62,200,727 LINC02339, PCDH20, 1 more genes
    nsv7058628inversion1nstd229human GRCh38 chr13: 61,211,116-61,885,145 , GRCh37.p13 chr13: 61,785,250-62,459,278 LINC02339, RAC1P8, 2 more genes
    nsv6955626copy number variation1nstd229human GRCh38 chr13: 61,405,487-61,408,810 , GRCh37.p13 chr13: 61,979,620-61,982,943 PCDH20
    nsv6952716copy number variation1nstd229human GRCh38 chr13: 61,349,430-62,117,406 , GRCh37.p13 chr13: 61,923,563-62,691,539 LINC02339, PCDH20, 3 more genes
    nsv6948548copy number variation1nstd229human GRCh38 chr13: 60,918,105-61,987,382 , GRCh37.p13 chr13: 61,492,239-62,561,515 LOC102723910, PCDH20, 5 more genes
    nsv6947987copy number variation1nstd229human GRCh38 chr13: 61,364,101-61,917,500 , GRCh37.p13 chr13: 61,938,234-62,491,633 LINC02339, PCDH20, 2 more genes
    nsv6938706copy number variation1nstd229human GRCh38 chr13: 61,386,851-61,435,001 , GRCh37.p13 chr13: 61,960,984-62,009,134 LINC02339, PCDH20
    nsv6637880copy number variation1nstd102humanUncertain significance GRCh37 chr13: 56,897,737-64,074,025 , GRCh38.p12 chr13: 56,323,603-63,499,892 DIAPH3-AS2, LOC107984625, 64 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
    nsv6576031inversion1nstd223human GRCh38 chr13: 61,211,116-61,885,145 , GRCh37.p13 chr13: 61,785,250-62,459,278 PCDH20, RAC1P8, 2 more genes
    nsv6483417copy number variation1nstd223human GRCh38 chr13: 61,411,357-61,412,082 , GRCh37.p13 chr13: 61,985,490-61,986,215 PCDH20
    nsv6475855copy number variation1nstd223human GRCh38 chr13: 60,554,208-61,958,462 , GRCh37.p13 chr13: 61,128,342-62,532,595 LOC105370231, RAC1P8, 12 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
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 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
    nsv6291752copy number variation1nstd102humanPathogenic GRCh37 chr13: 59,574,760-89,410,027 , GRCh38.p12 chr13: 59,000,626-88,757,773 GYG1P2, LOC102723968, 284 more genes
    nsv6291487copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921 CALM2P4, RNU6-81P, 778 more genes
    nsv6290319copy number variation1nstd102humanPathogenic GRCh37 chr13: 45,819,046-63,910,212 , GRCh38.p12 chr13: 45,244,911-63,336,079 CNMD, CPB2-AS1, 241 more genes
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