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Items: 1 to 20 of 133

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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
    nsv6880118copy number variation1nstd229human GRCh38 chr10: 70,152,586-70,152,786 , GRCh37.p13 chr10: 71,912,342-71,912,542 SAR1A
    nsv6878478copy number variation1nstd229human GRCh38 chr10: 70,144,322-70,149,221 , GRCh37.p13 chr10: 71,904,078-71,908,977 TYSND1, SAR1A
    nsv6449936copy number variation1nstd223human GRCh38 chr10: 69,592,739-70,157,404 , GRCh37.p13 chr10: 71,352,495-71,917,160 RPL5P26, SAR1A, 12 more genes
    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
    nsv6291213copy number variation1nstd102humanUncertain significance GRCh37 chr10: 71,754,361-72,399,690 , GRCh38.p12 chr10: 69,994,605-70,639,934 MACROH2A2, CEP57L1P1, 14 more genes
    nsv6131888copy number variation1nstd213human GRCh37 chr10: 71,890,000-72,730,001 , GRCh38.p12 chr10: 70,130,244-70,970,244 NPFFR1, TBATA, 18 more genes
    nsv6095540insertion1nstd212human GRCh38 chr10: 70,147,137-70,147,137 , GRCh37.p13 chr10: 71,906,893-71,906,893 SAR1A, TYSND1
    nsv5962587insertion1nstd209human GRCh38 chr10: 70,151,259-70,151,259 , GRCh37.p13 chr10: 71,911,015-71,911,015 SAR1A
    nsv5908235copy number variation1nstd209human GRCh38 chr10: 70,163,018-70,164,923 , GRCh37.p13 chr10: 71,922,774-71,924,679 SAR1A, CALM2P2
    nsv5848100copy number variation1nstd209human GRCh38 chr10: 70,163,013-70,164,812 , GRCh37.p13 chr10: 71,922,769-71,924,568 CALM2P2, SAR1A
    nsv5698980mobile element insertion1nstd211human GRCh38 chr10: 70,154,314-70,154,314 , GRCh37.p13 chr10: 71,914,070-71,914,070 SAR1A
    nsv5403223mobile element insertion1nstd206human GRCh38 chr10: 70,154,314-70,154,365 , GRCh37.p13 chr10: 71,914,070-71,914,121 SAR1A
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4601421copy number variation1nstd183human GRCh37 chr10: 70,564,120-74,122,461 , GRCh38.p12 chr10: 68,804,363-72,362,703 , SGPL1, 79 more genes
    nsv4487720mobile element insertion1nstd166human GRCh37.p13 chr10: 71,917,452-71,917,452 , GRCh38.p12 chr10: 70,157,696-70,157,696 SAR1A
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4187849copy number variation1nstd166human GRCh37.p13 chr10: 71,904,000-71,910,000 , GRCh38.p12 chr10: 70,144,244-70,150,244 TYSND1, SAR1A
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