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Items: 1 to 20 of 146

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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
    nsv6890797copy number variation1nstd229human GRCh38 chr10: 93,891,889-93,915,986 , GRCh37.p13 chr10: 95,651,646-95,675,743 SLC35G1
    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
    nsv6885019copy number variation1nstd229human GRCh38 chr10: 93,890,278-93,897,319 , GRCh37.p13 chr10: 95,650,035-95,657,076 SLC35G1
    nsv6882583copy number variation1nstd229human GRCh38 chr10: 93,895,475-93,941,668 , GRCh37.p13 chr10: 95,655,232-95,701,425 SLC35G1
    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
    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
    nsv6131820copy number variation1nstd213human GRCh37 chr10: 95,370,000-95,750,001 , GRCh38.p12 chr10: 93,610,243-93,990,244 PDE6C, LGI1, 7 more genes
    nsv6093816insertion1nstd212human GRCh38 chr10: 93,914,384-93,914,384 , GRCh37.p13 chr10: 95,674,141-95,674,141 SLC35G1
    nsv5960074insertion1nstd209human GRCh38 chr10: 93,914,384-93,914,384 , GRCh37.p13 chr10: 95,674,141-95,674,141 SLC35G1
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5916615copy number variation1nstd209human GRCh38 chr10: 93,876,944-93,938,329 , GRCh37.p13 chr10: 95,636,701-95,698,086 RAB11AP1, SLC35G1
    nsv5856314copy number variation1nstd209human GRCh38 chr10: 93,914,524-93,916,623 , GRCh37.p13 chr10: 95,674,281-95,676,380 SLC35G1
    nsv5855562copy number variation1nstd209human GRCh38 chr10: 93,876,302-93,915,623 , GRCh37.p13 chr10: 95,636,059-95,675,380 RAB11AP1, SLC35G1
    nsv5642054insertion1nstd207human GRCh38 chr10: 93,914,306-93,914,306 , GRCh37.p13 chr10: 95,674,063-95,674,063 SLC35G1
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