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Items: 1 to 20 of 229

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6957125copy number variation1nstd229human GRCh38 chr13: 37,573,397-37,573,427 , GRCh37.p13 chr13: 38,147,534-38,147,564 POSTN
    nsv6955062copy number variation1nstd229human GRCh38 chr13: 37,466,539-37,599,987 , GRCh37.p13 chr13: 38,040,676-38,174,124 POSTN, LINC01048, 1 more genes
    nsv6950453copy number variation1nstd229human GRCh38 chr13: 37,553,928-37,562,850 , GRCh37.p13 chr13: 38,128,065-38,136,987 POSTN
    nsv6942370copy number variation1nstd229human GRCh38 chr13: 37,460,406-37,561,471 , GRCh37.p13 chr13: 38,034,543-38,135,608 LINC00547, POSTN, 1 more genes
    nsv6941925copy number variation1nstd229human GRCh38 chr13: 37,577,918-37,581,954 , GRCh37.p13 chr13: 38,152,055-38,156,091 POSTN
    nsv6637985copy number variation1nstd102humanUncertain significance GRCh37 chr13: 36,148,057-41,670,428 , GRCh38.p12 chr13: 35,573,920-41,096,292 RPS12P24, SPART, 86 more genes
    nsv6637238copy number variation1nstd102humanPathogenic GRCh37 chr13: 35,501,428-40,901,176 , GRCh38.p12 chr13: 34,927,291-40,327,039 CCDC169-SOHLH2, RNA5SP26, 74 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
    nsv6490898copy number variation1nstd223human GRCh38 chr13: 37,598,930-37,599,624 , GRCh37.p13 chr13: 38,173,067-38,173,761 POSTN
    nsv6488662copy number variation1nstd223human GRCh38 chr13: 37,587,601-37,588,400 , GRCh37.p13 chr13: 38,161,738-38,162,537 POSTN
    nsv6478821copy number variation1nstd223human GRCh38 chr13: 37,562,401-37,574,300 , GRCh37.p13 chr13: 38,136,538-38,148,437 POSTN
    nsv6475644copy number variation1nstd223human GRCh38 chr13: 37,575,690-37,576,384 , GRCh37.p13 chr13: 38,149,827-38,150,521 POSTN
    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
    nsv6291701copy number variation1nstd102humanUncertain significance GRCh37 chr13: 37,464,566-38,493,263 , GRCh38.p12 chr13: 36,890,429-37,919,126 LINC00547, ALG5, 14 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6201539copy number variation1nstd214human GRCh38 chr13: 37,576,732-37,576,813 , GRCh37.p13 chr13: 38,150,869-38,150,950 POSTN
    nsv6132643copy number variation1nstd213human GRCh37 chr13: 38,010,000-38,490,001 , GRCh38.p12 chr13: 37,435,863-37,915,864 TRPC4, POSTN, 3 more genes
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