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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976348inversion1nstd209human GRCh38 chr4: 103,823,749-108,603,414 , GRCh37.p13 chr4: 104,744,906-109,524,570 , HADH, 54 more genes
    nsv5725620mobile element insertion2nstd211human GRCh38 chr4: 107,641,912-107,641,912 , GRCh37.p13 chr4: 108,563,068-108,563,068 PAPSS1
    nsv5691796mobile element insertion1nstd211human GRCh38 chr4: 107,660,138-107,660,138 , GRCh37.p13 chr4: 108,581,294-108,581,294 PAPSS1
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558603mobile element insertion1nstd206human GRCh38 chr4: 107,641,912-107,641,963 , GRCh37.p13 chr4: 108,563,068-108,563,119 PAPSS1
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5468328copy number variation1nstd206human GRCh38 chr4: 107,598,568-107,639,247 , GRCh37.p13 chr4: 108,519,724-108,560,403 , PAPSS1
    nsv5465622copy number variation1nstd206human GRCh38 chr4: 107,626,666-107,781,739 , GRCh37.p13 chr4: 108,547,822-108,702,895 PAPSS1
    nsv5164112mobile element insertion1nstd203human GRCh38 chr4: 107,641,895-107,641,912 , GRCh37.p13 chr4: 108,563,051-108,563,068 PAPSS1
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4935156copy number variation1nstd200human GRCh38 chr4: 107,619,754-107,622,682 , GRCh37.p13 chr4: 108,540,910-108,543,838 PAPSS1
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4794381copy number variation1nstd200human GRCh37 chr4: 108,133,484-108,580,713 , GRCh38.p12 chr4: 107,212,327-107,659,557 , LOC102725220, 3 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4587129copy number variation1nstd183human GRCh37 chr4: 108,577,994-108,578,394 , GRCh38.p12 chr4: 107,656,838-107,657,238 PAPSS1
    nsv4571630mobile element insertion1nstd166human GRCh37.p13 chr4: 108,563,051-108,563,051 , GRCh38.p12 chr4: 107,641,895-107,641,895 PAPSS1
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