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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv6896096copy number variation1nstd229human GRCh38 chr10: 94,088,127-94,090,391 , GRCh37.p13 chr10: 95,847,884-95,850,148 PLCE1-AS2, PLCE1
    nsv6890548copy number variation1nstd229human GRCh38 chr10: 93,867,543-94,344,766 , GRCh37.p13 chr10: 95,627,300-96,104,523 HDAC1P1, LOC107984255, 10 more genes
    nsv6878843copy number variation1nstd229human GRCh38 chr10: 94,107,901-94,111,900 , GRCh37.p13 chr10: 95,867,658-95,871,657 LOC107984255, PLCE1, 1 more genes
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6587941inversion1nstd223human GRCh38 chr10: 94,087,295-94,087,547 , GRCh37.p13 chr10: 95,847,052-95,847,304 PLCE1, PLCE1-AS2
    nsv6449173copy number variation1nstd223human GRCh38 chr10: 94,080,149-94,080,724 , GRCh37.p13 chr10: 95,839,906-95,840,481 PLCE1-AS2, PLCE1
    nsv6440566copy number variation1nstd223human GRCh38 chr10: 94,088,127-94,090,387 , GRCh37.p13 chr10: 95,847,884-95,850,144 PLCE1, PLCE1-AS2
    nsv6435851copy number variation1nstd223human GRCh38 chr10: 94,093,924-94,094,240 , GRCh37.p13 chr10: 95,853,681-95,853,997 PLCE1-AS2, PLCE1
    nsv6132060copy number variation1nstd213human GRCh37 chr10: 95,430,000-96,160,001 , GRCh38.p12 chr10: 93,670,243-94,400,244 LGI1, PLCE1, 14 more genes
    nsv6131986copy number variation1nstd213human GRCh37 chr10: 95,390,000-96,170,001 , GRCh38.p12 chr10: 93,630,243-94,410,244 PDE6C, LGI1, 16 more genes
    nsv6131898copy number variation1nstd213human GRCh37 chr10: 95,390,000-96,200,001 , GRCh38.p12 chr10: 93,630,243-94,440,244 PDE6C, LGI1, 16 more genes
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5907771copy number variation1nstd209human GRCh38 chr10: 94,093,924-94,094,239 , GRCh37.p13 chr10: 95,853,681-95,853,996 PLCE1, PLCE1-AS2
    nsv5718628mobile element insertion1nstd211human GRCh38 chr10: 94,095,581-94,095,581 , GRCh37.p13 chr10: 95,855,338-95,855,338 PLCE1-AS2, PLCE1
    nsv5584671copy number variation1nstd207human GRCh38 chr10: 94,093,924-94,094,239 , GRCh37.p13 chr10: 95,853,681-95,853,996 PLCE1, PLCE1-AS2
    nsv5476363copy number variation1nstd206human GRCh38 chr10: 94,093,938-94,094,240 , GRCh37.p13 chr10: 95,853,695-95,853,997 PLCE1-AS2, PLCE1
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