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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977899inversion1nstd209human GRCh38 chr2: 227,539,323-230,369,909 , GRCh37.p13 chr2: 228,404,039-231,234,624 , AGFG1, 40 more genes
    nsv5892367copy number variation1nstd209human GRCh38 chr2: 229,969,568-229,973,600 , GRCh37.p13 chr2: 230,834,284-230,838,316 RNU6-1027P, FBXO36
    nsv5891644copy number variation1nstd209human GRCh38 chr2: 229,971,924-229,972,243 , GRCh37.p13 chr2: 230,836,640-230,836,959 RNU6-1027P, FBXO36
    nsv5832801copy number variation1nstd209human GRCh38 chr2: 229,969,567-229,973,566 , GRCh37.p13 chr2: 230,834,283-230,838,282 FBXO36, RNU6-1027P
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5452672copy number variation1nstd206human GRCh38 chr2: 229,969,568-229,973,593 , GRCh37.p13 chr2: 230,834,284-230,838,309 RNU6-1027P, FBXO36
    nsv5450374copy number variation1nstd206human GRCh38 chr2: 229,848,423-230,038,610 , GRCh37.p13 chr2: 230,713,139-230,903,326 TRIP12, FBXO36, 6 more genes
    nsv5449024copy number variation1nstd206human GRCh38 chr2: 228,447,618-230,410,000 , GRCh37.p13 chr2: 229,312,334-231,274,715 , RPL7L1P10, 25 more genes
    nsv5444784copy number variation1nstd206human GRCh38 chr2: 229,923,868-230,024,854 , GRCh37.p13 chr2: 230,788,584-230,889,570 FBXO36, LOC105373924, 3 more genes
    nsv5366869translocation1nstd200human GRCh38 chr2: 229,969,624-229,969,624 , GRCh38 chr2: 229,973,592-229,973,592 , GRCh37.p13 chr2: 230,838,308-230,838,308 , GRCh37.p13 chr2: 230,834,340-230,834,340 RNU6-1027P, FBXO36
    nsv5309153copy number variation1nstd204human GRCh37.p13 chr2: 230,834,320-230,838,318 , GRCh38.p13 chr2: 229,969,604-229,973,602 RNU6-1027P, FBXO36
    nsv5306816copy number variation1nstd204human GRCh37.p13 chr2: 230,713,115-230,903,349 , GRCh38.p13 chr2: 229,848,399-230,038,633 TRIP12, FBXO36, 6 more genes
    nsv5214400copy number variation1nstd204human GRCh38.p13 chr2: 229,969,267-229,973,616 , GRCh37.p13 chr2: 230,833,983-230,838,332 FBXO36, RNU6-1027P
    nsv5212271copy number variation1nstd204human GRCh38.p13 chr2: 229,969,442-230,013,563 , GRCh37.p13 chr2: 230,834,158-230,878,279 FBXO36, RNU6-1027P
    nsv5206350copy number variation1nstd204human GRCh37.p13 chr2: 230,713,817-230,903,316 , GRCh38.p13 chr2: 229,849,101-230,038,600 TRIP12, FBXO36, 6 more genes
    nsv5203744copy number variation1nstd204human GRCh38.p13 chr2: 229,969,501-229,973,600 , GRCh37.p13 chr2: 230,834,217-230,838,316 RNU6-1027P, FBXO36
    nsv5039254inversion1nstd200human GRCh38 chr2: 227,539,122-230,370,113 , GRCh37.p13 chr2: 228,403,838-231,234,828 , LOC105373921, 40 more genes
    nsv4917305copy number variation1nstd200human GRCh38 chr2: 229,972,816-229,972,915 , GRCh37.p13 chr2: 230,837,532-230,837,631 FBXO36, RNU6-1027P
    nsv4917304copy number variation1nstd200human GRCh38 chr2: 229,963,264-229,972,129 , GRCh37.p13 chr2: 230,827,980-230,836,845 RNU6-1027P, FBXO36
    nsv4914026copy number variation1nstd200human GRCh38 chr2: 229,912,989-230,041,761 , GRCh37.p13 chr2: 230,777,705-230,906,477 TRIP12, FBXO36, 5 more genes
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