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Items: 1 to 20 of 424

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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
    nsv7069439inversion1nstd229human GRCh38 chr10: 10,500,497-12,439,947 , GRCh37.p13 chr10: 10,542,460-12,481,946 LOC105376409, SFTA1P, 26 more genes
    nsv7065461inversion1nstd229human GRCh38 chr10: 11,516,036-11,516,069 , GRCh37.p13 chr10: 11,558,035-11,558,068 LOC105376410, USP6NL
    nsv7061969inversion1nstd229human GRCh38 chr10: 11,128,019-14,526,691 , GRCh37.p13 chr10: 11,169,982-14,568,690 RPL5P25, LOC105376425, 58 more genes
    nsv6898035copy number variation1nstd229human GRCh38 chr10: 11,541,552-11,594,130 , GRCh37.p13 chr10: 11,583,551-11,636,129 USP6NL
    nsv6897394copy number variation1nstd229human GRCh38 chr10: 11,520,248-11,528,388 , GRCh37.p13 chr10: 11,562,247-11,570,387 USP6NL
    nsv6896414copy number variation1nstd229human GRCh38 chr10: 11,461,982-11,462,173 , GRCh37.p13 chr10: 11,503,981-11,504,172 LOC105376411, USP6NL
    nsv6895261copy number variation1nstd229human GRCh38 chr10: 11,547,969-11,548,059 , GRCh37.p13 chr10: 11,589,968-11,590,058 USP6NL
    nsv6893951copy number variation1nstd229human GRCh38 chr10: 11,556,101-11,559,200 , GRCh37.p13 chr10: 11,598,100-11,601,199 USP6NL
    nsv6892103copy number variation1nstd229human GRCh38 chr10: 11,483,578-11,486,836 , GRCh37.p13 chr10: 11,525,577-11,528,835 USP6NL
    nsv6887762copy number variation1nstd229human GRCh38 chr10: 11,549,375-11,556,663 , GRCh37.p13 chr10: 11,591,374-11,598,662 USP6NL
    nsv6887214copy number variation1nstd229human GRCh38 chr10: 11,452,279-11,452,334 , GRCh37.p13 chr10: 11,494,278-11,494,333 USP6NL
    nsv6886955copy number variation1nstd229human GRCh38 chr10: 11,478,401-11,480,469 , GRCh37.p13 chr10: 11,520,400-11,522,468 USP6NL
    nsv6885176copy number variation1nstd229human GRCh38 chr10: 11,536,374-11,548,305 , GRCh37.p13 chr10: 11,578,373-11,590,304 USP6NL
    nsv6884391copy number variation1nstd229human GRCh38 chr10: 11,537,165-11,546,456 , GRCh37.p13 chr10: 11,579,164-11,588,455 USP6NL
    nsv6884267copy number variation1nstd229human GRCh38 chr10: 11,526,898-11,527,240 , GRCh37.p13 chr10: 11,568,897-11,569,239 USP6NL
    nsv6879394copy number variation1nstd229human GRCh38 chr10: 11,477,057-11,477,099 , GRCh37.p13 chr10: 11,519,056-11,519,098 USP6NL
    nsv6637939copy number variation1nstd102humanUncertain significance GRCh37 chr10: 100,027-12,648,149 , GRCh38.p12 chr10: 54,087-12,606,150 LARP4B-DT, CALML5, 206 more genes
    nsv6637674copy number variation1nstd102humanUncertain significance GRCh37 chr10: 7,636,590-11,590,970 , GRCh38.p12 chr10: 7,594,627-11,548,971 HSP90AB7P, LOC105376394, 41 more genes
    nsv6620313copy number variation1nstd224human GRCh37 chr10: 11,237,928-11,729,374 , GRCh38.p12 chr10: 11,195,965-11,687,375 USP6NL, CELF2, 7 more genes
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