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Items: 1 to 20 of 122

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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
    nsv6894936copy number variation1nstd229human GRCh38 chr10: 93,282,047-93,286,040 , GRCh37.p13 chr10: 95,041,804-95,045,797 RPL17P34
    nsv6890277copy number variation1nstd229human GRCh38 chr10: 92,959,667-93,311,724 , GRCh37.p13 chr10: 94,719,424-95,071,481 MYOF, RPL17P34, 5 more genes
    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
    nsv6637218copy number variation1nstd102humanUncertain significance GRCh37 chr10: 94,970,750-95,184,396 , GRCh38.p12 chr10: 93,210,993-93,424,639 RPL17P34, MYOF
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6447371copy number variation1nstd223human GRCh38 chr10: 93,281,001-93,286,000 , GRCh37.p13 chr10: 95,040,758-95,045,757 RPL17P34
    nsv6441079copy number variation1nstd223human GRCh38 chr10: 93,284,678-93,285,134 , GRCh37.p13 chr10: 95,044,435-95,044,891 RPL17P34
    nsv6131819copy number variation1nstd213human GRCh37 chr10: 94,370,000-95,160,001 , GRCh38.p12 chr10: 92,610,243-93,400,244 CYP26A1, HHEX, 9 more genes
    nsv6123174copy number variation1nstd186human GRCh37 chr10: 95,041,664-95,045,803 , GRCh38.p12 chr10: 93,281,907-93,286,046 RPL17P34
    nsv6081354insertion1nstd212human GRCh38 chr10: 93,283,128-93,283,128 , GRCh37.p13 chr10: 95,042,885-95,042,885 RPL17P34
    nsv6001490copy number variation1nstd212human GRCh38 chr10: 93,282,109-93,285,851 , GRCh37.p13 chr10: 95,041,866-95,045,608 RPL17P34
    nsv5927067copy number variation1nstd209human GRCh38 chr10: 93,282,082-93,286,066 , GRCh37.p13 chr10: 95,041,839-95,045,823 RPL17P34
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5850612copy number variation1nstd209human GRCh38 chr10: 93,282,116-93,286,026 , GRCh37.p13 chr10: 95,041,873-95,045,783 RPL17P34
    nsv5492030copy number variation1nstd206human GRCh38 chr10: 93,281,907-93,286,046 , GRCh37.p13 chr10: 95,041,664-95,045,803 RPL17P34
    nsv5302285copy number variation1nstd204human GRCh38.p13 chr10: 93,282,043-93,285,996 , GRCh37.p13 chr10: 95,041,800-95,045,753 RPL17P34
    nsv5251407copy number variation1nstd204human GRCh38.p13 chr10: 93,280,901-93,286,100 , GRCh37.p13 chr10: 95,040,658-95,045,857 RPL17P34
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