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Items: 1 to 20 of 329

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7051353inversion1nstd229human GRCh38 chr2: 200,635,082-200,934,973 , GRCh37.p13 chr2: 201,499,805-201,799,696 NIF3L1, RNU6-312P, 15 more genes
    nsv7049459inversion1nstd229human GRCh38 chr2: 199,624,566-202,238,851 , GRCh37.p13 chr2: 200,489,289-203,103,574 LOC105373833, NDUFB3, 76 more genes
    nsv7047896inversion1nstd229human GRCh38 chr2: 200,658,909-200,660,458 , GRCh37.p13 chr2: 201,523,632-201,525,181 AOX1
    nsv6697182copy number variation1nstd229human GRCh38 chr2: 192,562,889-202,434,958 , GRCh37.p13 chr2: 193,427,615-203,299,681 RNU6-915P, SLC44A3P1, 150 more genes
    nsv6693821copy number variation1nstd229human GRCh38 chr2: 200,599,419-200,604,298 , GRCh37.p13 chr2: 201,464,142-201,469,021 AOX1
    nsv6693439copy number variation1nstd229human GRCh38 chr2: 200,648,903-200,651,575 , GRCh37.p13 chr2: 201,513,626-201,516,298 AOX1
    nsv6691917copy number variation1nstd229human GRCh38 chr2: 200,585,794-200,593,697 , GRCh37.p13 chr2: 201,450,517-201,458,420 AOX1
    nsv6691664copy number variation1nstd229human GRCh38 chr2: 200,654,935-200,655,635 , GRCh37.p13 chr2: 201,519,658-201,520,358 AOX1
    nsv6691299copy number variation1nstd229human GRCh38 chr2: 200,631,501-200,633,900 , GRCh37.p13 chr2: 201,496,224-201,498,623 AOX1
    nsv6689934copy number variation1nstd229human GRCh38 chr2: 200,392,938-200,607,376 , GRCh37.p13 chr2: 201,257,661-201,472,099 LOC101927741, SGO2, 3 more genes
    nsv6683514copy number variation1nstd229human GRCh38 chr2: 200,452,287-200,606,311 , GRCh37.p13 chr2: 201,317,010-201,471,034 SGO2, LOC101927741, 3 more genes
    nsv6681903copy number variation1nstd229human GRCh38 chr2: 200,610,623-200,611,096 , GRCh37.p13 chr2: 201,475,346-201,475,819 AOX1
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6634886copy number variation1nstd227human GRCh38.p12 chr2: 200,572,325-200,609,713 , GRCh37 chr2: 201,437,048-201,474,436 AOX1, SGO2
    nsv6627987copy number variation1nstd224human GRCh37 chr2: 201,462,135-201,499,556 , GRCh38.p12 chr2: 200,597,412-200,634,833 AOX1
    nsv6553752inversion1nstd223human GRCh38 chr2: 200,668,277-200,669,290 , GRCh37.p13 chr2: 201,533,000-201,534,013 AOX1
    nsv6352673copy number variation1nstd223human GRCh38 chr2: 200,599,419-200,604,298 , GRCh37.p13 chr2: 201,464,142-201,469,021 AOX1
    nsv6346509copy number variation1nstd223human GRCh38 chr2: 200,662,944-200,663,645 , GRCh37.p13 chr2: 201,527,667-201,528,368 AOX1
    nsv6341579copy number variation1nstd223human GRCh38 chr2: 200,651,199-200,651,839 , GRCh37.p13 chr2: 201,515,922-201,516,562 AOX1
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