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Items: 1 to 20 of 161

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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
    nsv6895764copy number variation1nstd229human GRCh38 chr10: 72,130,486-72,490,292 , GRCh37.p13 chr10: 73,890,244-74,250,050 SNX19P4, ASCC1, 6 more genes
    nsv6888988copy number variation1nstd229human GRCh38 chr10: 72,200,425-72,228,513 , GRCh37.p13 chr10: 73,960,183-73,988,271 ANAPC16, ASCC1
    nsv6878576copy number variation1nstd229human GRCh38 chr10: 72,230,440-72,232,999 , GRCh37.p13 chr10: 73,990,198-73,992,757 ANAPC16
    nsv6591294inversion1nstd223human GRCh38 chr10: 72,220,524-72,220,959 , GRCh37.p13 chr10: 73,980,282-73,980,717 ANAPC16
    nsv6584074inversion1nstd223human GRCh38 chr10: 72,234,011-72,235,146 , GRCh37.p13 chr10: 73,993,769-73,994,904 ANAPC16
    nsv6583199inversion1nstd223human GRCh38 chr10: 72,225,630-72,226,155 , GRCh37.p13 chr10: 73,985,388-73,985,913 ANAPC16
    nsv6581023inversion1nstd223human GRCh38 chr10: 72,231,731-72,232,114 , GRCh37.p13 chr10: 73,991,489-73,991,872 ANAPC16
    nsv6454783copy number variation1nstd223human GRCh38 chr10: 72,230,782-72,231,433 , GRCh37.p13 chr10: 73,990,540-73,991,191 ANAPC16
    nsv6452387copy number variation1nstd223human GRCh38 chr10: 72,235,097-72,236,638 , GRCh37.p13 chr10: 73,994,855-73,996,396 ANAPC16
    nsv6445924copy number variation1nstd223human GRCh38 chr10: 72,210,447-72,214,571 , GRCh37.p13 chr10: 73,970,205-73,974,329 ASCC1, ANAPC16
    nsv6439168copy number variation1nstd223human GRCh38 chr10: 72,232,053-72,237,386 , GRCh37.p13 chr10: 73,991,811-73,997,144 ANAPC16
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6247239mobile element insertion1nstd215human GRCh38 chr10: 72,233,530-72,233,530 , GRCh37.p13 chr10: 73,993,288-73,993,288 ANAPC16
    nsv6131970copy number variation1nstd213human GRCh37 chr10: 73,770,000-74,510,001 , GRCh38.p12 chr10: 72,010,242-72,750,243 CHST3, SPOCK2, 12 more genes
    nsv5965849insertion1nstd209human GRCh38 chr10: 72,218,166-72,218,166 , GRCh37.p13 chr10: 73,977,924-73,977,924 ASCC1, ANAPC16
    nsv5910963copy number variation1nstd209human GRCh38 chr10: 72,235,026-72,235,326 , GRCh37.p13 chr10: 73,994,784-73,995,084 ANAPC16
    nsv5708392mobile element insertion1nstd211human GRCh38 chr10: 72,218,166-72,218,166 , GRCh37.p13 chr10: 73,977,924-73,977,924 ASCC1, ANAPC16
    nsv5707530mobile element insertion2nstd211human GRCh38 chr10: 72,233,530-72,233,530 , GRCh37.p13 chr10: 73,993,288-73,993,288 ANAPC16
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