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Items: 1 to 20 of 335

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5908399copy number variation1nstd209human GRCh38 chr10: 102,556,626-102,556,971 , GRCh37.p13 chr10: 104,316,383-104,316,728 SUFU
    nsv5701128mobile element insertion1nstd211human GRCh38 chr10: 102,628,867-102,628,867 , GRCh37.p13 chr10: 104,388,624-104,388,624 SUFU
    nsv5672685copy number variation1nstd102humanPathogenic GRCh37 chr10: 104,352,329-104,352,491 , GRCh38.p12 chr10: 102,592,572-102,592,734 SUFU
    nsv5672605copy number variation1nstd102humanPathogenic GRCh37 chr10: 104,352,329-104,353,832 , GRCh38.p12 chr10: 102,592,572-102,594,075 SUFU
    nsv5669391inversion1nstd207human GRCh38 chr10: 102,611,074-102,620,416 , GRCh37.p13 chr10: 104,370,831-104,380,173 SUFU
    nsv5585955copy number variation1nstd207human GRCh38 chr10: 102,568,892-102,568,942 , GRCh37.p13 chr10: 104,328,649-104,328,699 SUFU
    nsv5512426copy number variation1nstd206human GRCh38 chr10: 102,529,573-102,531,211 , GRCh37.p13 chr10: 104,289,330-104,290,968 SUFU
    nsv5509516copy number variation1nstd206human GRCh38 chr10: 102,565,255-102,570,704 , GRCh37.p13 chr10: 104,325,012-104,330,461 SUFU, RPL23AP58
    nsv5508320copy number variation1nstd206human GRCh38 chr10: 102,556,606-102,557,012 , GRCh37.p13 chr10: 104,316,363-104,316,769 SUFU
    nsv5504661copy number variation1nstd206human GRCh38 chr10: 102,577,411-102,577,983 , GRCh37.p13 chr10: 104,337,168-104,337,740 SUFU
    nsv5474106copy number variation1nstd206human GRCh38 chr10: 102,518,513-102,518,583 , GRCh37.p13 chr10: 104,278,270-104,278,340 SUFU
    nsv5400835mobile element insertion1nstd206human GRCh38 chr10: 102,628,867-102,628,870 , GRCh37.p13 chr10: 104,388,624-104,388,627 SUFU
    nsv5380786copy number variation1nstd102humanPathogenic GRCh37 chr10: 104,386,922-104,392,580 , GRCh38.p12 chr10: 102,627,165-102,632,823 SUFU
    nsv5307608copy number variation1nstd204human GRCh38.p13 chr10: 102,585,734-102,588,059 , GRCh37.p13 chr10: 104,345,491-104,347,816 SUFU
    nsv5240498copy number variation1nstd204human GRCh38.p13 chr10: 102,610,401-102,681,200 , GRCh37.p13 chr10: 104,370,158-104,440,957 LOC105378460, TRIM8, 2 more genes
    nsv5192170mobile element insertion1nstd203human GRCh38 chr10: 102,513,884-102,513,904 , GRCh37.p13 chr10: 104,273,641-104,273,661 SUFU
    nsv5181373mobile element insertion1nstd203human GRCh38 chr10: 102,507,984-102,507,984 , GRCh37.p13 chr10: 104,267,741-104,267,741 SUFU
    nsv5138437mobile element insertion1nstd203human GRCh38 chr10: 102,527,588-102,527,603 , GRCh37.p13 chr10: 104,287,345-104,287,360 SUFU
    nsv5137203mobile element insertion1nstd203human GRCh38 chr10: 102,519,609-102,519,618 , GRCh37.p13 chr10: 104,279,366-104,279,375 SUFU
    nsv5129904mobile element insertion1nstd203human GRCh38 chr10: 102,541,697-102,541,721 , GRCh37.p13 chr10: 104,301,454-104,301,478 SUFU
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