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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094470copy number variation1nstd102humanUncertain significance GRCh37 chr15: 38,545,387-38,591,768 , GRCh38.p12 chr15: 38,253,186-38,299,567 SPRED1
    nsv7094368copy number variation1nstd102humanPathogenic GRCh37 chr15: 38,614,422-38,617,030 , GRCh38.p12 chr15: 38,322,221-38,324,829 SPRED1
    nsv7094284copy number variation1nstd102humanUncertain significance GRCh37 chr15: 38,591,554-38,643,865 , GRCh38.p12 chr15: 38,299,353-38,351,664 SPRED1
    nsv7094283copy number variation1nstd102humanPathogenic GRCh37 chr15: 38,545,387-38,545,438 , GRCh38.p12 chr15: 38,253,186-38,253,237 SPRED1
    nsv7093615insertion1nstd102humanUncertain significance GRCh38 chr15: 38,350,995-38,350,995 , GRCh37 chr15: 38,643,196-38,643,196 SPRED1
    nsv7077186inversion1nstd229human GRCh38 chr15: 35,051,912-40,816,689 , GRCh37.p13 chr15: 35,344,113-41,108,887 BUB1B-PAK6, LOC751603, 96 more genes
    nsv7069055inversion1nstd229human GRCh38 chr15: 37,465,340-38,788,853 , GRCh37.p13 chr15: 37,757,541-39,081,054 RASGRP1, LOC105370776, 12 more genes
    nsv7058209inversion1nstd229human GRCh38 chr15: 38,301,341-38,301,355 , GRCh37.p13 chr15: 38,593,542-38,593,556 SPRED1
    nsv6977336copy number variation1nstd229human GRCh38 chr15: 38,284,565-38,284,664 , GRCh37.p13 chr15: 38,576,766-38,576,865 SPRED1
    nsv6967073copy number variation1nstd229human GRCh38 chr15: 38,165,382-38,652,921 , GRCh37.p13 chr15: 38,457,583-38,945,122 LOC100422645, SPRED1, 3 more genes
    nsv6515110copy number variation1nstd223human GRCh38 chr15: 38,293,601-38,294,600 , GRCh37.p13 chr15: 38,585,802-38,586,801 SPRED1
    nsv6513101copy number variation1nstd223human GRCh38 chr15: 38,333,305-38,333,983 , GRCh37.p13 chr15: 38,625,506-38,626,184 SPRED1
    nsv6512940copy number variation1nstd223human GRCh38 chr15: 38,351,267-38,351,626 , GRCh37.p13 chr15: 38,643,468-38,643,827 SPRED1
    nsv6512877copy number variation1nstd223human GRCh38 chr15: 38,332,690-38,333,261 , GRCh37.p13 chr15: 38,624,891-38,625,462 SPRED1
    nsv6512560copy number variation1nstd223human GRCh38 chr15: 38,300,201-38,301,300 , GRCh37.p13 chr15: 38,592,402-38,593,501 SPRED1
    nsv6509841copy number variation1nstd223human GRCh38 chr15: 38,311,814-38,312,548 , GRCh37.p13 chr15: 38,604,015-38,604,749 SPRED1
    nsv6509347copy number variation1nstd223human GRCh38 chr15: 38,295,601-38,296,600 , GRCh37.p13 chr15: 38,587,802-38,588,801 SPRED1
    nsv6505389copy number variation1nstd223human GRCh38 chr15: 38,279,504-38,280,104 , GRCh37.p13 chr15: 38,571,705-38,572,305 SPRED1
    nsv6504048copy number variation1nstd223human GRCh38 chr15: 38,313,501-38,314,600 , GRCh37.p13 chr15: 38,605,702-38,606,801 SPRED1
    nsv6503969copy number variation1nstd223human GRCh38 chr15: 38,338,501-38,339,600 , GRCh37.p13 chr15: 38,630,702-38,631,801 SPRED1
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