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Items: 1 to 20 of 291

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060146inversion1nstd229human GRCh38 chr13: 70,704,220-75,002,513 , GRCh37.p13 chr13: 71,278,352-75,576,650 RNU4-10P, LOC107987191, 39 more genes
    nsv6956688copy number variation1nstd229human GRCh38 chr13: 72,087,667-72,831,428 , GRCh37.p13 chr13: 72,661,805-73,405,566 MZT1, BORA, 5 more genes
    nsv6948899copy number variation1nstd229human GRCh38 chr13: 72,025,801-74,742,700 , GRCh37.p13 chr13: 72,599,939-75,316,837 RNU6-66P, RNY1P8, 28 more genes
    nsv6948687copy number variation1nstd229human GRCh38 chr13: 72,695,213-72,757,292 , GRCh37.p13 chr13: 73,269,351-73,331,430 RPL21P110, BORA, 3 more genes
    nsv6948017copy number variation1nstd229human GRCh38 chr13: 72,725,501-72,726,200 , GRCh37.p13 chr13: 73,299,639-73,300,338 MZT1, BORA
    nsv6946941copy number variation1nstd229human GRCh38 chr13: 72,743,921-72,872,089 , GRCh37.p13 chr13: 73,318,059-73,446,227 PIBF1, BORA, 1 more genes
    nsv6944228copy number variation1nstd229human GRCh38 chr13: 72,677,686-72,761,790 , GRCh37.p13 chr13: 73,251,824-73,335,928 MZT1, BORA, 3 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
    nsv6621958copy number variation1nstd224human GRCh37 chr13: 73,283,184-73,547,734 , GRCh38.p12 chr13: 72,709,046-72,973,596 DIS3, PIBF1, 3 more genes
    nsv6491544copy number variation1nstd223human GRCh38 chr13: 72,738,265-72,738,838 , GRCh37.p13 chr13: 73,312,403-73,312,976 BORA
    nsv6480466copy number variation1nstd223human GRCh38 chr13: 72,725,459-72,726,167 , GRCh37.p13 chr13: 73,299,597-73,300,305 MZT1, BORA
    nsv6479995copy number variation1nstd223human GRCh38 chr13: 72,743,920-72,872,088 , GRCh37.p13 chr13: 73,318,058-73,446,226 BORA, PIBF1, 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
    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
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6249280mobile element insertion1nstd215human GRCh38 chr13: 72,726,762-72,726,762 , GRCh37.p13 chr13: 73,300,900-73,300,900 BORA, MZT1
    nsv6133106copy number variation1nstd213human GRCh37 chr13: 73,200,000-73,360,001 , GRCh38.p12 chr13: 72,625,862-72,785,863 PIBF1, DIS3, 4 more genes
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