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Items: 1 to 20 of 414

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141420insertion1nstd232human GRCh37.p13 chr10: 99,034,873-99,034,873 , GRCh38.p12 chr10: 97,275,116-97,275,116 ARHGAP19, ARHGAP19-SLIT1
    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
    nsv7071816inversion1nstd229human GRCh38 chr10: 97,269,060-97,269,133 , GRCh37.p13 chr10: 99,028,817-99,028,890 ARHGAP19-SLIT1, ARHGAP19
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6896463copy number variation1nstd229human GRCh38 chr10: 97,255,316-97,256,859 , GRCh37.p13 chr10: 99,015,073-99,016,616 ARHGAP19-SLIT1, ARHGAP19
    nsv6895684copy number variation1nstd229human GRCh38 chr10: 97,258,463-97,265,413 , GRCh37.p13 chr10: 99,018,220-99,025,170 ARHGAP19, ARHGAP19-SLIT1
    nsv6887786copy number variation1nstd229human GRCh38 chr10: 97,266,010-97,281,007 , GRCh37.p13 chr10: 99,025,767-99,040,764 ARHGAP19, ARHGAP19-SLIT1
    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
    nsv6885329copy number variation1nstd229human GRCh38 chr10: 97,253,301-97,260,800 , GRCh37.p13 chr10: 99,013,058-99,020,557 ARHGAP19, ARHGAP19-SLIT1
    nsv6884870copy number variation1nstd229human GRCh38 chr10: 97,241,130-97,244,233 , GRCh37.p13 chr10: 99,000,887-99,003,990 ARHGAP19, ARHGAP19-SLIT1
    nsv6881535copy number variation1nstd229human GRCh38 chr10: 97,075,720-97,243,650 , GRCh37.p13 chr10: 98,835,477-99,003,407 ARHGAP19, SLIT1-AS1, 4 more genes
    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
    nsv6594465inversion1nstd223human GRCh38 chr10: 97,288,005-97,288,990 , GRCh37.p13 chr10: 99,047,762-99,048,747 ARHGAP19, ARHGAP19-SLIT1
    nsv6594223inversion1nstd223human GRCh38 chr10: 97,237,638-97,238,437 , GRCh37.p13 chr10: 98,997,395-98,998,194 ARHGAP19, ARHGAP19-SLIT1
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