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Items: 1 to 20 of 123

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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
    nsv5691851mobile element insertion1nstd211human GRCh38 chr4: 105,813,916-105,813,916 , GRCh37.p13 chr4: 106,735,073-106,735,073 GSTCD, GSTCD-AS1
    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
    nsv5311340copy number variation1nstd204human GRCh38.p13 chr4: 103,868,735-105,953,170 , GRCh37.p13 chr4: 104,789,892-106,874,327 CXXC4, GSTCD, 23 more genes
    nsv5239082copy number variation1nstd204human GRCh38.p13 chr4: 104,702,601-105,953,500 , GRCh37.p13 chr4: 105,623,758-106,874,657 LOC107986190, RNU6-553P, 18 more genes
    nsv5223021copy number variation1nstd204human GRCh38.p13 chr4: 105,823,140-105,832,753 , GRCh37.p13 chr4: 106,744,297-106,753,910 GSTCD, GSTCD-AS1
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4935102copy number variation1nstd200human GRCh38 chr4: 105,812,941-105,822,058 , GRCh37.p13 chr4: 106,734,098-106,743,215 GSTCD, GSTCD-AS1
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4801012copy number variation1nstd200human GRCh37 chr4: 106,734,098-106,743,215 , GRCh38.p12 chr4: 105,812,941-105,822,058 GSTCD, GSTCD-AS1
    nsv4800964copy number variation1nstd200human GRCh37 chr4: 104,789,902-106,874,324 , GRCh38.p12 chr4: 103,868,745-105,953,167 RNU6-553P, RNU6-351P, 23 more genes
    nsv4794374copy number variation1nstd200human GRCh37 chr4: 106,703,330-106,840,570 , GRCh38.p12 chr4: 105,782,173-105,919,413 GSTCD-AS1, NPNT, 2 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
    nsv4589453copy number variation1nstd183human GRCh37 chr4: 106,699,705-106,747,257 , GRCh38.p12 chr4: 105,778,548-105,826,100 GSTCD, GSTCD-AS1, 1 more genes
    nsv4567603mobile element insertion1nstd166human GRCh37.p13 chr4: 106,740,238-106,740,238 , GRCh38.p12 chr4: 105,819,081-105,819,081 GSTCD, GSTCD-AS1
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