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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
    nsv7056673inversion1nstd229human GRCh38 chr2: 200,789,164-201,081,461 , GRCh37.p13 chr2: 201,653,887-201,946,184 ORC2, CLK1, 17 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
    nsv7044131inversion1nstd229human GRCh38 chr2: 200,766,186-201,065,779 , GRCh37.p13 chr2: 201,630,909-201,930,502 AOX3P-AOX2P, HYCC2, 16 more genes
    nsv7040451inversion1nstd229human GRCh38 chr2: 201,058,970-201,059,075 , GRCh37.p13 chr2: 201,923,693-201,923,798 HYCC2
    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
    nsv6696612copy number variation1nstd229human GRCh38 chr2: 201,067,901-201,120,900 , GRCh37.p13 chr2: 201,932,624-201,985,623 RNU6-1206P, RPL17P10, 4 more genes
    nsv6695885copy number variation1nstd229human GRCh38 chr2: 201,024,104-201,024,570 , GRCh37.p13 chr2: 201,888,827-201,889,293 HYCC2
    nsv6693877copy number variation1nstd229human GRCh38 chr2: 201,004,205-201,004,576 , GRCh37.p13 chr2: 201,868,928-201,869,299 LOC105373835, HYCC2
    nsv6691352copy number variation1nstd229human GRCh38 chr2: 201,045,437-201,056,719 , GRCh37.p13 chr2: 201,910,160-201,921,442 HYCC2
    nsv6681161copy number variation1nstd229human GRCh38 chr2: 201,002,070-201,008,505 , GRCh37.p13 chr2: 201,866,793-201,873,228 LOC105373835, HYCC2
    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
    nsv6555374inversion1nstd223human GRCh38 chr2: 201,025,229-201,025,391 , GRCh37.p13 chr2: 201,889,952-201,890,114 HYCC2
    nsv6555039inversion1nstd223human GRCh38 chr2: 200,993,890-200,994,434 , GRCh37.p13 chr2: 201,858,613-201,859,157 LOC105373835, HYCC2
    nsv6553260inversion1nstd223human GRCh38 chr2: 200,999,387-200,999,845 , GRCh37.p13 chr2: 201,864,110-201,864,568 HYCC2, LOC105373835
    nsv6549787inversion1nstd223human GRCh38 chr2: 200,990,886-200,991,319 , GRCh37.p13 chr2: 201,855,609-201,856,042 LOC105373835, HYCC2
    nsv6549301inversion1nstd223human GRCh38 chr2: 201,039,988-201,040,760 , GRCh37.p13 chr2: 201,904,711-201,905,483 HYCC2
    nsv6546990inversion1nstd223human GRCh38 chr2: 201,031,417-201,031,933 , GRCh37.p13 chr2: 201,896,140-201,896,656 HYCC2
    nsv6539050inversion1nstd223human GRCh38 chr2: 200,984,251-200,985,036 , GRCh37.p13 chr2: 201,848,974-201,849,759 HYCC2, LOC105373835
    nsv6354969copy number variation1nstd223human GRCh38 chr2: 201,036,701-201,042,400 , GRCh37.p13 chr2: 201,901,424-201,907,123 HYCC2
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