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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv5968661insertion1nstd209human GRCh38 chr15: 93,038,569-93,038,569 , GRCh37.p13 chr15: 93,581,799-93,581,799 RGMA
    nsv5946177copy number variation1nstd209human GRCh38 chr15: 93,046,794-93,046,868 , GRCh37.p13 chr15: 93,590,024-93,590,098 RGMA
    nsv5531310copy number variation1nstd206human GRCh38 chr15: 93,046,796-93,046,863 , GRCh37.p13 chr15: 93,590,026-93,590,093 RGMA
    nsv5531067copy number variation1nstd206human GRCh38 chr15: 92,402,520-97,547,707 , GRCh37.p13 chr15: 92,945,750-98,090,937 , LOC105371004, 71 more genes
    nsv5380847copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr15: 93,444,468-93,583,743 , GRCh38.p12 chr15: 92,901,238-93,040,513 CHD2, RGMA, 1 more genes
    nsv5365426translocation1nstd200human GRCh38 chr15: 93,089,891-93,089,891 , GRCh38 chr15: 93,088,685-93,088,685 , GRCh37.p13 chr15: 93,631,914-93,631,914 , GRCh37.p13 chr15: 93,633,120-93,633,120 LOC101927025, RGMA
    nsv5365425translocation1nstd200human GRCh38 chr15: 93,088,685-93,088,685 , GRCh38 chr15: 93,089,616-93,089,616 , GRCh37.p13 chr15: 93,631,914-93,631,914 , GRCh37.p13 chr15: 93,632,845-93,632,845 LOC101927025, RGMA
    nsv5349303translocation1nstd200human GRCh38 chr15: 93,046,796-93,046,796 , GRCh38 chr15: 93,046,863-93,046,863 , GRCh37.p13 chr15: 93,590,026-93,590,026 , GRCh37.p13 chr15: 93,590,093-93,590,093 RGMA
    nsv5325125translocation1nstd204human GRCh37.p13 chr15: 93,632,764-93,632,764 , GRCh37.p13 chr15: 93,632,834-93,632,834 , GRCh38.p13 chr15: 93,089,535-93,089,535 , GRCh38.p13 chr15: 93,089,605-93,089,605 RGMA, LOC101927025
    nsv5319928copy number variation1nstd204human GRCh38.p13 chr15: 92,922,305-93,117,174 , GRCh37.p13 chr15: 93,465,535-93,660,403 LOC101927025, RGMA, 2 more genes
    nsv5274348copy number variation1nstd204human GRCh38.p13 chr15: 93,018,163-93,058,958 , GRCh37.p13 chr15: 93,561,393-93,602,187 CHD2, RGMA
    nsv5261074copy number variation1nstd204human GRCh38.p13 chr15: 92,922,301-93,117,100 , GRCh37.p13 chr15: 93,465,531-93,660,329 YBX2P2, CHD2, 2 more genes
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4683982copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,444,448-93,583,743 , GRCh38.p12 chr15: 92,901,218-93,040,513 MIR3175, CHD2, 1 more genes
    nsv4675851copy number variation1nstd102humanUncertain significance GRCh37 chr15: 93,373,121-93,747,449 , GRCh38.p12 chr15: 92,829,891-93,204,220 CHD2, YBX2P2, 5 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4674927copy number variation1nstd102humanUncertain significance GRCh37 chr15: 93,451,635-93,885,876 , GRCh38.p12 chr15: 92,908,405-93,342,647 LOC105370982, RGMA, 4 more genes
    nsv4625078copy number variation1nstd183human GRCh37 chr15: 93,576,982-93,589,740 , GRCh38.p12 chr15: 93,033,752-93,046,510 RGMA
    nsv4565103sequence alteration1nstd166human GRCh37.p13 chr15: 93,631,912-93,633,103 , GRCh38.p12 chr15: 93,088,683-93,089,874 RGMA, LOC101927025
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