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Items: 1 to 20 of 112

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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
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6886722copy number variation1nstd229human GRCh38 chr10: 97,320,001-97,390,200 , GRCh37.p13 chr10: 99,079,758-99,149,957 RRP12, LOC105378448, 2 more genes
    nsv6885955copy number variation1nstd229human GRCh38 chr10: 97,182,219-97,365,920 , GRCh37.p13 chr10: 98,941,976-99,125,677 RRP12, LOC105378447, 8 more genes
    nsv6884890copy number variation1nstd229human GRCh38 chr10: 97,298,418-97,320,022 , GRCh37.p13 chr10: 99,058,175-99,079,779 RPL12P27, FRAT1
    nsv6881411copy number variation1nstd229human GRCh38 chr10: 97,282,801-97,378,900 , GRCh37.p13 chr10: 99,042,558-99,138,657 RRP12, ARHGAP19, 5 more genes
    nsv6880682copy number variation1nstd229human GRCh38 chr10: 97,224,366-98,323,209 , GRCh37.p13 chr10: 98,984,123-100,082,966 ZDHHC16, RPL34P20, 29 more genes
    nsv6880393copy number variation1nstd229human GRCh38 chr10: 97,245,070-97,586,825 , GRCh37.p13 chr10: 99,004,827-99,346,582 LOC644215, ARHGAP19, 14 more genes
    nsv6637978copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,027,360-99,300,723 , GRCh38.p12 chr10: 97,267,603-97,540,966 RPL12P27, ARHGAP19-SLIT1, 12 more genes
    nsv6620786copy number variation1nstd224human GRCh37 chr10: 98,942,021-99,116,903 , GRCh38.p12 chr10: 97,182,264-97,357,146 RPL12P27, FRAT2, 8 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6451320copy number variation1nstd223human GRCh38 chr10: 97,317,901-97,321,600 , GRCh37.p13 chr10: 99,077,658-99,081,357 FRAT1
    nsv6314071copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,070,594-99,445,724 , GRCh38.p12 chr10: 97,310,837-97,685,967 AVPI1, ANKRD2, 15 more genes
    nsv6131821copy number variation1nstd213human GRCh37 chr10: 98,490,000-99,090,001 , GRCh38.p12 chr10: 96,730,243-97,330,244 SLIT1, FRAT1, 12 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
    nsv5348024translocation1nstd200human GRCh38 chr10: 97,320,019-97,320,019 , GRCh38 chr10: 97,298,418-97,298,418 , GRCh37.p13 chr10: 99,079,776-99,079,776 , GRCh37.p13 chr10: 99,058,175-99,058,175 FRAT1
    nsv5334680translocation1nstd200human GRCh37 chr10: 99,079,776-99,079,776 , GRCh37 chr10: 99,058,175-99,058,175 , GRCh38.p12 chr10: 97,320,019-97,320,019 , GRCh38.p12 chr10: 97,298,418-97,298,418 FRAT1
    nsv4973938copy number variation1nstd200human GRCh38 chr10: 97,271,421-97,343,975 , GRCh37.p13 chr10: 99,031,178-99,103,732 FRAT2, ARHGAP19, 4 more genes
    nsv4542318insertion1nstd166human GRCh37.p13 chr10: 99,081,532-99,081,532 , GRCh38.p12 chr10: 97,321,775-97,321,775 FRAT1
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