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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3988136copy number variation3estd229human GRCh37 chr20: 29,423,716-29,500,566 , GRCh38.p12 chr20: 30,189,040-30,265,890 CFTRP3
    esv3981730copy number variation4estd229human GRCh37 chr6: 78,967,351-79,036,200 , GRCh38.p12 chr6: 78,257,634-78,326,483 LOC105377865
    esv3981493copy number variation18estd229human GRCh37 chr6: 32,454,901-32,508,000 , GRCh38.p12 chr6: 32,487,124-32,540,223 HLA-DRB5
    esv3988067copy number variation8estd229human GRCh37 chr4: 34,779,601-34,829,100 , GRCh38.p12 chr4: 34,777,979-34,827,478 , GRCh38.p12 chr4|NW_003315915.1: 270,308-319,807 LOC105378262
    esv3983899copy number variation1estd229human GRCh37 chr11: 49,710,151-49,757,850 , GRCh38.p12 chr11: 49,688,599-49,736,298 , GRCh38.p12 chr11|NW_019805495.1: 152,781-200,447 GRM5P1
    esv3988779copy number variation6estd229human GRCh37 chr4: 49,588,812-49,628,667 , GRCh38.p12 chr4: 49,586,795-49,626,650 SNX18P25
    esv3981340copy number variation3estd229human GRCh37 chr6: 171,002,701-171,034,650 , GRCh38.p12 chr6: 170,693,613-170,725,562 LOC101929692
    esv3988143copy number variation1estd229human GRCh37 chr20: 29,566,903-29,598,493 , GRCh38.p12 chr20: 30,332,227-30,363,817 FAM242A
    esv3981962copy number variation3estd229human GRCh37 chr7: 141,765,301-141,794,550 , GRCh38.p12 chr7: 142,065,501-142,094,750 , GRCh38.p12 chr7|NT_187562.1: 27,381-56,630 MGAM
    esv3986887copy number variation2estd229human GRCh37 chr10: 49,304,251-49,328,100 , GRCh38.p12 chr10: 48,096,208-48,120,057 PTPN20CP
    esv3987975copy number variation8estd229human GRCh37 chr10: 124,360,201-124,378,200 , GRCh38.p12 chr10: 122,600,685-122,618,684 DMBT1
    esv3989990copy number variation1estd229human GRCh37 chr4: 76,103,045-76,119,783 , GRCh38.p12 chr4: 75,177,835-75,194,573 LOC100506253
    esv3987799copy number variation5estd229human GRCh37 chr19: 40,371,301-40,387,950 , GRCh38.p12 chr19: 39,880,661-39,897,310 , GRCh38.p12 chr19|NW_009646206.1: 140,537-157,186 FCGBP
    esv3986333copy number variation7estd229human GRCh37 chr10: 100,687,951-100,701,900 , GRCh38.p12 chr10: 98,928,194-98,942,143 HPSE2
    esv3982734copy number variation1estd229human GRCh37 chr8: 12,453,301-12,466,350 , GRCh38.p12 chr8: 12,595,792-12,608,841 , GRCh38.p12 chr8|NW_018654717.1: 5,791,208-5,804,255 LOC729732
    esv3981936copy number variation3estd229human GRCh37 chr7: 133,785,001-133,798,050 , GRCh38.p12 chr7: 134,100,248-134,113,297
    esv3986001copy number variation1estd229human GRCh37 chr15: 102,420,001-102,432,600 , GRCh38.p12 chr15: 101,879,798-101,892,397 WBP1LP5
    esv3987125copy number variation4estd229human GRCh37 chr17: 43,650,451-43,662,600 , GRCh38.p12 chr17: 45,573,085-45,585,234 , GRCh38.p12 chr17|NT_187663.1: 275,224-287,373 LRRC37A3, DND1P1
    esv3981343copy number variation5estd229human GRCh37 chr6: 171,039,151-171,051,300 , GRCh38.p12 chr6: 170,730,063-170,742,212 LOC101929692
    esv3977271copy number variation1estd229human GRCh37 chr5: 177,389,551-177,401,250 , GRCh38.p12 chr5: 177,962,550-177,974,249 , GRCh38.p12 chr5|NT_187546.1: 100,350-111,868 , GRCh38.p12 chr5|NT_187652.1: 97,086-108,791 SUDS3P1
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