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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5464023copy number variation1nstd206human GRCh38 chr5: 110,989,807-111,303,807 , GRCh37.p13 chr5: 110,325,506-110,639,505 CAMK4, TSLP, 4 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4932218copy number variation1nstd200human GRCh38 chr5: 111,062,188-111,086,226 , GRCh37.p13 chr5: 110,397,886-110,421,924 TSLP
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4803406copy number variation1nstd200human GRCh37 chr5: 110,397,886-110,421,924 , GRCh38.p12 chr5: 111,062,188-111,086,226 TSLP
    nsv4729561copy number variation1nstd102humanUncertain significance GRCh37 chr5: 110,338,499-110,668,272 , GRCh38.p12 chr5: 111,002,800-111,332,574 LOC100129099, WDR36, 4 more genes
    nsv4589730copy number variation1nstd183human GRCh37 chr5: 110,334,818-110,420,356 , GRCh38.p12 chr5: 110,999,119-111,084,658 LOC105379121, TSLP
    nsv4589617copy number variation1nstd183human GRCh37 chr5: 110,411,863-110,413,545 , GRCh38.p12 chr5: 111,076,165-111,077,847 TSLP
    nsv4456071copy number variation1nstd102humanPathogenic GRCh37 chr5: 108,304,806-121,335,239 , GRCh38.p12 chr5: 108,969,105-121,999,544 HMGN1P13, LOC101927023, 153 more genes
    nsv4455983copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,949,118-129,317,455 , GRCh38.p12 chr5: 90,653,301-129,981,762 LOC345576, LOC107986436, 419 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4397728copy number variation1nstd174human GRCh37 chr5: 110,405,317-110,458,508 , GRCh38.p12 chr5: 111,069,619-111,122,810 TSLP, WDR36
    nsv4374189copy number variation1nstd173human GRCh37 chr5: 110,411,136-110,442,228 , GRCh38.p12 chr5: 111,075,438-111,106,529 WDR36, TSLP
    nsv4365606copy number variation2nstd173human GRCh37 chr5: 110,307,856-110,427,052 , GRCh38.p12 chr5: 110,972,157-111,091,354 TSLP, WDR36, 2 more genes
    nsv4321173inversion1nstd166human GRCh37.p13 chr5: 86,365,040-130,339,409 , GRCh38.p12 chr5: 87,069,223-131,003,716 , APC, 481 more genes
    nsv4117799copy number variation1nstd166human GRCh37.p13 chr5: 110,406,439-110,555,995 , GRCh38.p12 chr5: 111,070,741-111,220,297 TSLP, LOC100129099, 2 more genes
    nsv4115136copy number variation1nstd166human GRCh37.p13 chr5: 110,391,266-110,424,086 , GRCh38.p12 chr5: 111,055,568-111,088,388 TSLP
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