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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094477copy number variation1nstd102humanUncertain significance GRCh37 chr13: 41,367,363-43,181,054 , GRCh38.p12 chr13: 40,793,227-42,606,918 CYCSP34, RN7SL597P, 42 more genes
    nsv7076983inversion1nstd229human GRCh38 chr13: 41,990,578-41,998,945 , GRCh37.p13 chr13: 42,564,714-42,573,081 LOC105370176
    nsv7075189inversion1nstd229human GRCh38 chr13: 38,938,572-45,892,931 , GRCh37.p13 chr13: 39,512,709-46,467,066 TPT1-AS1, AKAP11, 136 more genes
    nsv7073451inversion1nstd229human GRCh38 chr13: 39,843,646-49,674,098 , GRCh37.p13 chr13: 40,417,783-50,248,234 CYCSP34, FNDC3A, 195 more genes
    nsv7063213inversion1nstd229human GRCh38 chr13: 39,276,739-42,681,969 , GRCh37.p13 chr13: 39,850,876-43,256,105 TPTE2P5, KBTBD7, 63 more genes
    nsv7060789inversion1nstd229human GRCh38 chr13: 38,967,784-43,058,064 , GRCh37.p13 chr13: 39,541,921-43,632,200 RGCC, RAC1P3, 79 more genes
    nsv6952483copy number variation1nstd229human GRCh38 chr13: 41,848,658-47,157,739 , GRCh37.p13 chr13: 42,422,794-47,731,874 TSC22D1-AS1, LINC00330, 105 more genes
    nsv6952424copy number variation1nstd229human GRCh38 chr13: 41,708,259-42,230,367 , GRCh37.p13 chr13: 42,282,395-42,804,503 RNU6-74P, KARS1P1, 8 more genes
    nsv6949692copy number variation1nstd229human GRCh38 chr13: 41,979,240-41,987,769 , GRCh37.p13 chr13: 42,553,376-42,561,905 LOC105370176, VWA8-AS1
    nsv6947654copy number variation1nstd229human GRCh38 chr13: 42,013,095-42,014,258 , GRCh37.p13 chr13: 42,587,231-42,588,394 LOC105370176
    nsv6947594copy number variation1nstd229human GRCh38 chr13: 42,012,156-42,020,145 , GRCh37.p13 chr13: 42,586,292-42,594,281 LOC105370176
    nsv6938681copy number variation1nstd229human GRCh38 chr13: 41,986,001-41,998,600 , GRCh37.p13 chr13: 42,560,137-42,572,736 LOC105370176
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6593490inversion1nstd223human GRCh38 chr13: 41,974,172-41,975,311 , GRCh37.p13 chr13: 42,548,308-42,549,447 VWA8-AS1, LOC105370176
    nsv6584656inversion1nstd223human GRCh38 chr13: 41,974,135-41,975,226 , GRCh37.p13 chr13: 42,548,271-42,549,362 LOC105370176, VWA8-AS1
    nsv6580174inversion1nstd223human GRCh38 chr13: 41,987,943-41,988,722 , GRCh37.p13 chr13: 42,562,079-42,562,858 LOC105370176
    nsv6484287copy number variation1nstd223human GRCh38 chr13: 42,000,179-42,000,652 , GRCh37.p13 chr13: 42,574,315-42,574,788 LOC105370176
    nsv6479683copy number variation1nstd223human GRCh38 chr13: 41,983,248-41,983,767 , GRCh37.p13 chr13: 42,557,384-42,557,903 LOC105370176
    nsv6476229copy number variation1nstd223human GRCh38 chr13: 41,997,642-41,998,212 , GRCh37.p13 chr13: 42,571,778-42,572,348 LOC105370176
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
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