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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969033inversion1nstd209human GRCh38 chr4: 108,267,752-117,667,772 , GRCh37.p13 chr4: 109,188,908-118,588,927 , ANK2, 134 more genes
    nsv5679107mobile element insertion1nstd211human GRCh38 chr4: 109,720,614-109,720,614 , GRCh37.p13 chr4: 110,641,770-110,641,770 PLA2G12A
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5367752translocation1nstd200human GRCh38 chr4: 109,725,209-109,725,209 , GRCh38 chrX: 11,934,865-11,934,865 , GRCh37.p13 chrX: 11,952,984-11,952,984 , GRCh37.p13 chr4: 110,646,365-110,646,365 PLA2G12A, FRMPD4
    nsv5345951translocation1nstd200human GRCh37 chrX: 11,952,984-11,952,984 , GRCh37 chr4: 110,646,365-110,646,365 , GRCh38.p12 chrX: 11,934,865-11,934,865 , GRCh38.p12 chr4: 109,725,209-109,725,209 FRMPD4, PLA2G12A
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4935231copy number variation1nstd200human GRCh38 chr4: 109,727,332-109,750,151 , GRCh37.p13 chr4: 110,648,488-110,671,307 PLA2G12A, CFI
    nsv4935230copy number variation1nstd200human GRCh38 chr4: 109,709,406-109,709,492 , GRCh37.p13 chr4: 110,630,562-110,630,648 PLA2G12A
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 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
    nsv4455413copy number variation1nstd102humanUncertain significance GRCh37 chr4: 110,386,827-110,660,498 , GRCh38.p12 chr4: 109,465,671-109,739,342 CASP6, SETP20, 7 more genes
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv4328272inversion1nstd166human GRCh37.p13 chr4: 110,343,023-114,944,660 , GRCh38.p12 chr4: 109,421,867-114,023,504 , EGF, 82 more genes
    nsv4110160copy number variation1nstd166human GRCh37.p13 chr4: 110,647,730-110,651,689 , GRCh38.p12 chr4: 109,726,574-109,730,533 CFI, PLA2G12A
    nsv4095600copy number variation1nstd166human GRCh37.p13 chr4: 110,633,926-110,648,551 , GRCh38.p12 chr4: 109,712,770-109,727,395 PLA2G12A
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