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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144433insertion1nstd232human GRCh37.p13 chr5: 142,675,155-142,675,155 , GRCh38.p12 chr5: 143,295,590-143,295,590 NR3C1
    nsv7056804inversion1nstd229human GRCh38 chr5: 142,173,020-146,166,895 , GRCh37.p13 chr5: 141,552,585-145,546,458 GRXCR2, LARS1, 38 more genes
    nsv7045608inversion1nstd229human GRCh38 chr5: 142,902,498-151,105,008 , GRCh37.p13 chr5: 142,282,063-150,484,569 FBXO38-DT, POU4F3, 126 more genes
    nsv7044204inversion1nstd229human GRCh38 chr5: 143,418,449-143,421,975 , GRCh37.p13 chr5: 142,798,014-142,801,540 NR3C1
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6794789copy number variation1nstd229human GRCh38 chr5: 143,435,395-143,440,193 , GRCh37.p13 chr5: 142,814,960-142,819,758 NR3C1
    nsv6794679copy number variation1nstd229human GRCh38 chr5: 143,284,671-143,290,814 , GRCh37.p13 chr5: 142,664,236-142,670,379 NR3C1
    nsv6794469copy number variation1nstd229human GRCh38 chr5: 143,363,601-143,368,900 , GRCh37.p13 chr5: 142,743,166-142,748,465 NR3C1
    nsv6792507copy number variation1nstd229human GRCh38 chr5: 143,350,596-143,359,703 , GRCh37.p13 chr5: 142,730,161-142,739,268 NR3C1
    nsv6791132copy number variation1nstd229human GRCh38 chr5: 143,398,638-143,399,155 , GRCh37.p13 chr5: 142,778,203-142,778,720 NR3C1
    nsv6789985copy number variation1nstd229human GRCh38 chr5: 143,381,178-143,395,735 , GRCh37.p13 chr5: 142,760,743-142,775,300 NR3C1
    nsv6788388copy number variation1nstd229human GRCh38 chr5: 143,340,328-143,342,766 , GRCh37.p13 chr5: 142,719,893-142,722,331 NR3C1
    nsv6787404copy number variation1nstd229human GRCh38 chr5: 143,417,452-143,417,630 , GRCh37.p13 chr5: 142,797,017-142,797,195 NR3C1
    nsv6783989copy number variation1nstd229human GRCh38 chr5: 143,286,091-143,286,322 , GRCh37.p13 chr5: 142,665,656-142,665,887 NR3C1
    nsv6783121copy number variation1nstd229human GRCh38 chr5: 143,297,000-143,297,145 , GRCh37.p13 chr5: 142,676,565-142,676,710 NR3C1
    nsv6780794copy number variation1nstd229human GRCh38 chr5: 143,151,301-143,391,200 , GRCh37.p13 chr5: 142,530,866-142,770,765 ARHGAP26, NR3C1, 2 more genes
    nsv6780454copy number variation1nstd229human GRCh38 chr5: 142,838,521-146,873,932 , GRCh37.p13 chr5: 142,218,086-146,253,495 RPL35AP17, KRT8P48, 43 more genes
    nsv6779580copy number variation1nstd229human GRCh38 chr5: 143,427,135-143,432,549 , GRCh37.p13 chr5: 142,806,700-142,812,114 NR3C1
    nsv6779547copy number variation1nstd229human GRCh38 chr5: 143,360,639-143,364,488 , GRCh37.p13 chr5: 142,740,204-142,744,053 NR3C1
    nsv6778779copy number variation1nstd229human GRCh38 chr5: 143,314,995-143,336,261 , GRCh37.p13 chr5: 142,694,560-142,715,826 RPL7P21, NR3C1
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