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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054431inversion1nstd229human GRCh38 chr4: 108,267,754-117,667,771 , GRCh37.p13 chr4: 109,188,910-118,588,926 , MIR297, 128 more genes
    nsv6756472copy number variation1nstd229human GRCh38 chr4: 108,742,963-108,752,982 , GRCh37.p13 chr4: 109,664,119-109,674,138 ETNPPL
    nsv6752801copy number variation1nstd229human GRCh38 chr4: 108,545,189-108,916,249 , GRCh37.p13 chr4: 109,466,345-109,837,405 RPL34, ETNPPL, 6 more genes
    nsv6749849copy number variation1nstd229human GRCh38 chr4: 103,966,147-109,668,724 , GRCh37.p13 chr4: 104,887,304-110,589,880 CYP2U1-AS1, OSTC, 66 more genes
    nsv6749816copy number variation1nstd229human GRCh38 chr4: 108,753,779-108,753,803 , GRCh37.p13 chr4: 109,674,935-109,674,959 ETNPPL
    nsv6744301copy number variation1nstd229human GRCh38 chr4: 108,744,974-108,746,786 , GRCh37.p13 chr4: 109,666,130-109,667,942 ETNPPL
    nsv6743621copy number variation1nstd229human GRCh38 chr4: 108,494,149-109,149,255 , GRCh37.p13 chr4: 109,415,305-110,070,411 RNU6-431P, COL25A1, 6 more genes
    nsv6742187copy number variation1nstd229human GRCh38 chr4: 108,722,923-108,787,556 , GRCh37.p13 chr4: 109,644,079-109,708,712 RCC2P8, ETNPPL
    nsv6739137copy number variation1nstd229human GRCh38 chr4: 107,868,481-108,740,935 , GRCh37.p13 chr4: 108,789,637-109,662,091 LEF1-AS1, ZACNP1, 15 more genes
    nsv6573675inversion1nstd223human GRCh38 chr4: 108,753,516-108,754,008 , GRCh37.p13 chr4: 109,674,672-109,675,164 ETNPPL
    nsv6572140inversion1nstd223human GRCh38 chr4: 108,267,752-117,667,773 , GRCh37.p13 chr4: 109,188,908-118,588,928 , RPS26P25, 128 more genes
    nsv6556222inversion1nstd223human GRCh38 chr4: 108,711,905-115,978,756 , GRCh37.p13 chr4: 109,633,061-116,899,912 , MIR577, 98 more genes
    nsv6393173copy number variation1nstd223human GRCh38 chr4: 108,736,340-108,741,300 , GRCh37.p13 chr4: 109,657,496-109,662,456 ETNPPL
    nsv6390953copy number variation1nstd223human GRCh38 chr4: 108,722,923-108,787,555 , GRCh37.p13 chr4: 109,644,079-109,708,711 RCC2P8, ETNPPL
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291428copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060 ADH1A, ADH1B, 157 more genes
    nsv6263860copy number variation1nstd214human GRCh38 chr4: 108,747,181-108,747,238 , GRCh37.p13 chr4: 109,668,337-109,668,394 ETNPPL
    nsv6263764copy number variation1nstd214human GRCh38 chr4: 108,747,148-108,747,253 , GRCh37.p13 chr4: 109,668,304-109,668,409 ETNPPL
    nsv6263659copy number variation1nstd214human GRCh38 chr4: 108,747,178-108,747,238 , GRCh37.p13 chr4: 109,668,334-109,668,394 ETNPPL
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