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Items: 1 to 20 of 556

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 ACTL7B, OR13C3, 88 more genes
    nsv7098191copy number variation1nstd102humanUncertain significance GRCh37 chr9: 107,546,596-108,536,361 , GRCh38.p12 chr9: 104,784,315-105,774,080 TMEM38B, CT70, 14 more genes
    nsv7075341inversion1nstd229human GRCh38 chr9: 105,329,198-105,332,595 , GRCh37.p13 chr9: 108,091,479-108,094,876 SLC44A1
    nsv7070339inversion1nstd229human GRCh38 chr9: 105,335,156-105,335,256 , GRCh37.p13 chr9: 108,097,437-108,097,537 SLC44A1
    nsv7062784inversion1nstd229human GRCh38 chr9: 105,247,017-105,897,262 , GRCh37.p13 chr9: 108,009,298-108,659,543 SLC44A1, RALGAPA1P1, 9 more genes
    nsv6877981copy number variation1nstd229human GRCh38 chr9: 105,246,382-105,250,730 , GRCh37.p13 chr9: 108,008,663-108,013,011 LOC112268038, SLC44A1
    nsv6877196copy number variation1nstd229human GRCh38 chr9: 105,362,246-105,362,764 , GRCh37.p13 chr9: 108,124,527-108,125,045 SLC44A1
    nsv6876687copy number variation1nstd229human GRCh38 chr9: 105,296,801-105,299,600 , GRCh37.p13 chr9: 108,059,082-108,061,881 SLC44A1
    nsv6873669copy number variation1nstd229human GRCh38 chr9: 105,351,568-105,351,668 , GRCh37.p13 chr9: 108,113,849-108,113,949 SLC44A1
    nsv6871379copy number variation1nstd229human GRCh38 chr9: 105,436,206-105,444,263 , GRCh37.p13 chr9: 108,198,487-108,206,544 SLC44A1, FSD1L
    nsv6870270copy number variation1nstd229human GRCh38 chr9: 105,300,345-105,301,006 , GRCh37.p13 chr9: 108,062,626-108,063,287 SLC44A1
    nsv6869269copy number variation1nstd229human GRCh38 chr9: 105,310,014-105,318,854 , GRCh37.p13 chr9: 108,072,295-108,081,135 SLC44A1
    nsv6869053copy number variation1nstd229human GRCh38 chr9: 105,316,938-105,320,846 , GRCh37.p13 chr9: 108,079,219-108,083,127 SLC44A1
    nsv6868096copy number variation1nstd229human GRCh38 chr9: 105,292,749-105,295,118 , GRCh37.p13 chr9: 108,055,030-108,057,399 SLC44A1
    nsv6868087copy number variation1nstd229human GRCh38 chr9: 105,407,108-105,419,836 , GRCh37.p13 chr9: 108,169,389-108,182,117 SLC44A1
    nsv6866154copy number variation1nstd229human GRCh38 chr9: 105,252,291-105,252,325 , GRCh37.p13 chr9: 108,014,572-108,014,606 SLC44A1
    nsv6863582copy number variation1nstd229human GRCh38 chr9: 105,436,905-105,538,929 , GRCh37.p13 chr9: 108,199,186-108,301,210 SLC44A1, RALGAPA1P1, 1 more genes
    nsv6863296copy number variation1nstd229human GRCh38 chr9: 105,275,763-105,278,751 , GRCh37.p13 chr9: 108,038,044-108,041,032 SLC44A1
    nsv6861871copy number variation1nstd229human GRCh38 chr9: 105,318,655-105,328,799 , GRCh37.p13 chr9: 108,080,936-108,091,080 SLC44A1
    nsv6859816copy number variation1nstd229human GRCh38 chr9: 105,439,442-105,439,461 , GRCh37.p13 chr9: 108,201,723-108,201,742 SLC44A1
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