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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5926909copy number variation1nstd209human GRCh38 chr10: 133,345,536-133,346,598 , GRCh37.p13 chr10: 135,159,040-135,160,102 PRAP1
    nsv5856655copy number variation1nstd209human GRCh38 chr10: 133,334,104-133,346,209 , GRCh37.p13 chr10: 135,147,608-135,159,713 PRAP1, CALY, 1 more genes
    nsv5712080mobile element insertion1nstd211human GRCh38 chr10: 133,345,879-133,345,879 , GRCh37.p13 chr10: 135,159,383-135,159,383 PRAP1
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5505165copy number variation1nstd206human GRCh38 chr10: 133,345,496-133,346,639 , GRCh37.p13 chr10: 135,159,000-135,160,143 PRAP1
    nsv5504019copy number variation1nstd206human GRCh38 chr10: 133,200,862-133,379,746 , GRCh37.p13 chr10: 135,014,366-135,193,250 MIR202HG, VENTX, 14 more genes
    nsv5499281copy number variation1nstd206human GRCh38 chr10: 133,322,800-133,368,000 , GRCh37.p13 chr10: 135,136,304-135,181,504 ECHS1, PRAP1, 3 more genes
    nsv5404686mobile element insertion1nstd206human GRCh38 chr10: 133,345,879-133,345,930 , GRCh37.p13 chr10: 135,159,383-135,159,434 PRAP1
    nsv5381769copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,483,682-135,434,178 , GRCh38.p12 chr10: 127,685,418-133,620,674 DPYSL4, LINC02667, 88 more genes
    nsv5255637copy number variation1nstd204human GRCh38.p13 chr10: 133,292,501-133,426,700 , GRCh37.p13 chr10: 135,106,005-135,240,204 BANF1P2, FUOM, 9 more genes
    nsv5243065copy number variation1nstd204human GRCh38.p13 chr10: 133,327,863-133,367,819 , GRCh37.p13 chr10: 135,141,367-135,181,323 FUOM, BANF1P2, 3 more genes
    nsv4984081copy number variation1nstd200human GRCh38 chr10: 133,346,604-133,601,248 , GRCh37.p13 chr10: 135,160,108-135,414,752 , OR7M1P, 15 more genes
    nsv4984080copy number variation1nstd200human GRCh38 chr10: 133,345,536-133,346,599 , GRCh37.p13 chr10: 135,159,040-135,160,103 PRAP1
    nsv4984079copy number variation1nstd200human GRCh38 chr10: 133,340,667-133,373,667 , GRCh37.p13 chr10: 135,154,171-135,187,171 FUOM, BANF1P2, 3 more genes
    nsv4984078copy number variation1nstd200human GRCh38 chr10: 133,339,475-133,432,353 , GRCh37.p13 chr10: 135,152,979-135,245,857 OR6L2P, PRAP1, 7 more genes
    nsv4984060copy number variation1nstd200human GRCh38 chr10: 132,934,989-133,515,554 , GRCh37.p13 chr10: 134,748,493-135,329,058 , SCART1, 33 more genes
    nsv4729670copy number variation1nstd102humanPathogenic GRCh37 chr10: 129,031,265-135,427,143 , GRCh38.p12 chr10: 127,233,001-133,613,639 LOC105378561, LINC01164, 91 more genes
    nsv4729448copy number variation1nstd102humanLikely benign GRCh37 chr10: 135,165,733-135,427,143 , GRCh38.p12 chr10: 133,352,229-133,613,639 LOC105378575, OR7M1P, 13 more genes
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