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Items: 1 to 20 of 557

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122554copy number variation1nstd186human GRCh37 chr15: 83,275,277-83,275,581 , GRCh38.p12 chr15: 82,606,528-82,606,831 , GRCh38.p12 chr15|NT_187606.1: 395,632-395,936 CPEB1
    nsv6115712copy number variation1nstd186human GRCh37 chr15: 83,165,721-83,170,120 , GRCh38.p12 chr15: 82,497,000-82,501,399 , GRCh38.p12 chr15|NT_187606.1: 286,076-290,475 GOLGA2P10
    nsv5385053mobile element deletion1nstd186human GRCh37 chr15: 83,275,284-83,275,581 , GRCh38.p12 chr15: 82,606,535-82,606,831 , GRCh38.p12 chr15|NT_187606.1: 395,639-395,936 CPEB1
    nsv5382224mobile element deletion1nstd186human GRCh37 chr15: 83,275,285-83,275,581 , GRCh38.p12 chr15|NT_187606.1: 395,640-395,936 , GRCh38.p12 chr15: 82,606,536-82,606,831 CPEB1
    nsv4856080copy number variation1nstd200human GRCh37 chr15: 83,303,440-83,314,289 , GRCh38.p12 chr15|NT_187606.1: 423,795-430,880 , GRCh38.p12 chr15: 82,634,689-82,641,774 CPEB1
    nsv4856078copy number variation1nstd200human GRCh37 chr15: 83,272,231-83,277,776 , GRCh38.p12 chr15: 82,603,482-82,609,026 , GRCh38.p12 chr15|NT_187606.1: 392,586-398,131 CPEB1
    nsv4856077copy number variation1nstd200human GRCh37 chr15: 83,245,210-83,248,514 , GRCh38.p12 chr15|NT_187606.1: 365,565-368,869 , GRCh38.p12 chr15: 82,576,460-82,579,764 CPEB1
    nsv4785983mobile element deletion1nstd200human GRCh37 chr15: 83,275,285-83,275,581 , GRCh38.p12 chr15|NT_187606.1: 395,640-395,936 , GRCh38.p12 chr15: 82,606,536-82,606,831 CPEB1
    nsv4744733copy number variation1nstd199human GRCh37 chr15: 83,290,116-83,292,172 , GRCh38.p12 chr15: 82,621,365-82,623,421 , GRCh38.p12 chr15|NT_187606.1: 410,471-412,527 CPEB1
    nsv4730603copy number variation1nstd199human GRCh37 chr15: 83,275,279-83,275,590 , GRCh38.p12 chr15: 82,606,530-82,606,840 , GRCh38.p12 chr15|NT_187606.1: 395,634-395,945 CPEB1
    nsv4714732copy number variation1nstd195human GRCh37 chr15: 83,033,551-83,034,251 , GRCh38.p12 chr15: 82,364,823-82,365,523 , GRCh38.p12 chr15|NT_187606.1: 153,906-154,606 UBE2Q2P2
    nsv4711136copy number variation2nstd195human GRCh37 chr15: 83,275,270-83,275,271 , GRCh38.p12 chr15: 82,606,521-82,606,522 , GRCh38.p12 chr15|NT_187606.1: 395,625-395,626 CPEB1
    nsv4706224copy number variation1nstd195human GRCh37 chr15: 83,166,001-83,170,201 , GRCh38.p12 chr15: 82,497,280-82,501,485 , GRCh38.p12 chr15|NT_187606.1: 286,356-290,556 GOLGA2P10
    nsv4670494copy number variation1nstd186human GRCh37 chr15: 82,938,571-83,023,464 , GRCh38.p12 chr15|NT_187606.1: 58,926-143,819 UBE2Q2P11, LOC440300, 9 more genes
    nsv4651703copy number variation1nstd186human GRCh37 chr15: 83,108,750-83,124,000 , GRCh38.p12 chr15: 82,440,025-82,455,302 , GRCh38.p12 chr15|NT_187606.1: 229,105-244,355 DNM1P36, UBE2Q2P6, 1 more genes
    nsv4650783copy number variation1nstd186human GRCh37 chr15: 82,922,000-82,928,000 , GRCh38.p12 chr15|NT_187606.1: 42,355-48,355 ADAMTS7P1, DNM1P43
    nsv4650294copy number variation4nstd186human GRCh37 chr15: 83,003,000-83,008,000 , GRCh38.p12 chr15|NT_187606.1: 123,355-128,355 DNM1P41, GOLGA6L4, 2 more genes
    nsv4648040copy number variation1nstd186human GRCh37 chr15: 82,974,000-82,979,000 , GRCh38.p12 chr15|NT_187606.1: 94,355-99,355 GOLGA2P7, LOC440300, 1 more genes
    nsv4647377copy number variation1nstd186human GRCh37 chr15: 83,139,000-83,149,000 , GRCh38.p12 chr15|NT_187606.1: 259,355-269,355 , GRCh38.p12 chr15: 82,470,278-82,480,272 CSPG4P10, GOLGA2P10
    nsv4646258copy number variation1nstd186human GRCh37 chr15: 82,914,000-82,928,300 , GRCh38.p12 chr15|NT_187606.1: 34,355-48,655 ADAMTS7P1, DNM1P43
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