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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5939686copy number variation1nstd209human GRCh38 chr17: 28,265,920-28,267,272 , GRCh37.p13 chr17: 26,592,946-26,594,298 LOC101926984
    nsv5560937sequence alteration1nstd206human GRCh38 chr17: 28,266,717-28,266,827 , GRCh37.p13 chr17: 26,593,743-26,593,853 LOC101926984
    nsv5556615sequence alteration1nstd206human GRCh38 chr17: 28,265,933-28,266,077 , GRCh37.p13 chr17: 26,592,959-26,593,103 LOC101926984
    nsv5531642copy number variation1nstd206human GRCh38 chr17: 28,267,471-28,268,723 , GRCh37.p13 chr17: 26,594,497-26,595,749 LOC101926984
    nsv5529320copy number variation1nstd206human GRCh38 chr17: 28,265,366-28,266,132 , GRCh37.p13 chr17: 26,592,392-26,593,158 LOC101926984
    nsv5526212copy number variation1nstd206human GRCh38 chr17: 28,266,668-28,269,143 , GRCh37.p13 chr17: 26,593,694-26,596,169 LOC101926984
    nsv5521074copy number variation1nstd206human GRCh38 chr17: 28,250,952-28,263,413 , GRCh37.p13 chr17: 26,577,978-26,590,439 LOC101926984, LOC105371712
    nsv5330778translocation1nstd200human GRCh37 chr17: 26,596,381-26,596,381 , GRCh37 chr17: 26,596,092-26,596,092 , GRCh38.p12 chr17: 28,269,355-28,269,355 , GRCh38.p12 chr17: 28,269,066-28,269,066 LOC101926984
    nsv5323370copy number variation1nstd204human GRCh37.p13 chr17: 26,577,967-26,590,447 , GRCh38.p13 chr17: 28,250,941-28,263,421 LOC105371712, LOC101926984
    nsv5321989copy number variation1nstd204human GRCh38.p13 chr17: 28,267,380-28,268,677 , GRCh37.p13 chr17: 26,594,406-26,595,703 LOC101926984
    nsv5294764copy number variation1nstd204human GRCh38.p13 chr17: 28,251,001-28,263,300 , GRCh37.p13 chr17: 26,578,027-26,590,326 LOC105371712, LOC101926984
    nsv5194805mobile element insertion1nstd203human GRCh38 chr17: 28,271,300-28,271,315 , GRCh37.p13 chr17: 26,598,326-26,598,341 LOC101926984
    nsv5010240copy number variation1nstd200human GRCh38 chr17: 28,250,952-28,263,413 , GRCh37.p13 chr17: 26,577,978-26,590,439 LOC101926984, LOC105371712
    nsv4858452copy number variation1nstd200human GRCh37 chr17: 26,594,556-26,595,694 , GRCh38.p12 chr17: 28,267,530-28,268,668 LOC101926984
    nsv4858451copy number variation1nstd200human GRCh37 chr17: 26,594,270-26,594,990 , GRCh38.p12 chr17: 28,267,244-28,267,964 LOC101926984
    nsv4858450copy number variation1nstd200human GRCh37 chr17: 26,577,978-26,590,439 , GRCh38.p12 chr17: 28,250,952-28,263,413 LOC105371712, LOC101926984
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4732138copy number variation1nstd199human GRCh37 chr17: 26,594,890-26,595,632 , GRCh38.p12 chr17: 28,267,864-28,268,606 LOC101926984
    nsv4675321copy number variation1nstd102humanPathogenic GRCh37 chr17: 25,274,363-28,450,707 , GRCh38.p12 chr17: 26,947,337-30,123,689 ABHD15, LOC100420408, 112 more genes
    nsv4573684mobile element insertion1nstd166human GRCh37.p13 chr17: 26,589,614-26,589,614 , GRCh38.p12 chr17: 28,262,588-28,262,588 LOC101926984
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