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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142756insertion1nstd232human GRCh37.p13 chr10: 92,631,832-92,631,832 , GRCh38.p12 chr10: 90,872,075-90,872,075 RPP30
    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
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7066197inversion1nstd229human GRCh38 chr10: 90,423,055-91,029,089 , GRCh37.p13 chr10: 92,182,812-92,788,846 RPP30, HTR7, 5 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6893491copy number variation1nstd229human GRCh38 chr10: 90,884,100-90,888,053 , GRCh37.p13 chr10: 92,643,857-92,647,810 RPP30
    nsv6890617copy number variation1nstd229human GRCh38 chr10: 90,906,010-90,916,604 , GRCh37.p13 chr10: 92,665,767-92,676,361 ANKRD1, RPP30
    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
    nsv6637708copy number variation1nstd102humanUncertain significance GRCh37 chr10: 92,549,833-92,657,760 , GRCh38.p12 chr10: 90,790,076-90,898,003 RPP30, HTR7
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6275777insertion1nstd214human GRCh38 chr10: 90,880,116-90,880,116 , GRCh37.p13 chr10: 92,639,873-92,639,873 RPP30
    nsv6131984copy number variation1nstd213human GRCh37 chr10: 92,240,000-92,800,001 , GRCh38.p12 chr10: 90,480,243-91,040,244 HTR7, RPP30, 6 more genes
    nsv5559614sequence alteration1nstd206human GRCh38 chr10: 90,881,868-90,881,962 , GRCh37.p13 chr10: 92,641,625-92,641,719 RPP30
    nsv5138309mobile element insertion1nstd203human GRCh38 chr10: 90,871,448-90,871,457 , GRCh37.p13 chr10: 92,631,205-92,631,214 RPP30
    nsv5131493mobile element insertion1nstd203human GRCh38 chr10: 90,892,056-90,892,071 , GRCh37.p13 chr10: 92,651,813-92,651,828 RPP30
    nsv5125146mobile element insertion1nstd203human GRCh38 chr10: 90,871,444-90,871,453 , GRCh37.p13 chr10: 92,631,201-92,631,210 RPP30
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4675983copy number variation1nstd102humanUncertain significance GRCh37 chr10: 92,614,401-92,722,894 , GRCh38.p12 chr10: 90,854,644-90,963,137 HTR7, XLOC_008559, 3 more genes
    nsv4547731insertion1nstd166human GRCh37.p13 chr10: 92,641,625-92,641,625 , GRCh38.p12 chr10: 90,881,868-90,881,868 RPP30
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