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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5226228copy number variation1nstd204human GRCh38.p13 chr4: 190,016,261-190,024,132 , GRCh37.p13 chr4: 190,937,416-190,945,287 , GRCh37.p13 chr4|NW_003571034.1: 109,191-117,062 RNA5SP175, FRG2, 1 more genes
    nsv4944215copy number variation1nstd200human GRCh38 chr4: 189,981,469-190,036,339 , GRCh37.p13 chr4|NW_003571034.1: 74,399-129,269 , GRCh37.p13 chr4: 190,902,624-190,957,494 TUBB7P, FRG2, 4 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
    nsv4728932copy number variation1nstd102humanPathogenic GRCh37 chr4: 187,391,214-190,957,473 , GRCh38.p12 chr4: 186,470,060-190,036,318 F11-AS1, LOC102723906, 57 more genes
    nsv4715453copy number variation3nstd195human GRCh37 chr4: 190,940,951-190,943,951 , GRCh38.p12 chr4: 190,019,796-190,022,796 , GRCh38.p12 chr4|NT_187650.1: 357,327-360,327 FRG2, DUX4L9
    nsv4715077copy number variation1nstd195human GRCh37 chr4: 190,940,951-190,944,201 , GRCh38.p12 chr4: 190,019,796-190,023,046 , GRCh38.p12 chr4|NT_187650.1: 357,327-360,577 FRG2, DUX4L9
    nsv4706237translocation1nstd195human GRCh37 chr4: 190,941,328-190,941,328 , GRCh37 chr9: 66,454,896-66,454,896 , GRCh38.p12 chr4: 190,020,173-190,020,173 , GRCh38.p12 chr9: 62,799,072-62,799,072 , GRCh38.p12 chr4|NT_187650.1: 357,704-357,704 DUX4L9
    nsv4703678translocation1nstd195human GRCh37 chr4: 190,941,328-190,941,328 , GRCh37 chr9: 66,454,897-66,454,897 , GRCh38.p12 chr4: 190,020,173-190,020,173 , GRCh38.p12 chr9: 62,799,073-62,799,073 , GRCh38.p12 chr4|NT_187650.1: 357,704-357,704 DUX4L9
    nsv4680593copy number variation1nstd189human GRCh37.p13 chr4: 190,022,496-191,154,276 , GRCh38.p12 chr4: 189,101,342-190,123,121 FRG1, HSP90AA4P, 28 more genes
    nsv4680309copy number variation1nstd189human GRCh37.p13 chr4: 190,417,468-191,154,276 , GRCh38.p12 chr4: 189,496,314-190,123,121 FRG1, DUX4L1, 25 more genes
    nsv4680216copy number variation1nstd189human GRCh37.p13 chr4: 189,929,465-191,154,276 , GRCh38.p12 chr4: 189,008,311-190,123,121 FRG1, HSP90AA4P, 30 more genes
    nsv4679147copy number variation1nstd189human GRCh37.p13 chr4: 190,127,883-191,154,276 , GRCh38.p12 chr4: 189,206,729-190,123,121 FRG1, HSP90AA4P, 27 more genes
    nsv4674658copy number variation1nstd102humanPathogenic GRCh37 chr4: 178,566,256-190,957,473 , GRCh38.p12 chr4: 177,645,102-190,036,318 RARRES2P4, ING2-DT, 165 more genes
    nsv4674043copy number variation1nstd102humanPathogenic GRCh37 chr4: 165,010,461-190,957,473 , GRCh38.p12 chr4: 164,089,309-190,036,318 CYP4V2, ZFP42, 319 more genes
    nsv4663890copy number variation1nstd186human GRCh37 chr4: 190,916,698-191,009,730 , GRCh38.p12 chr4: 189,995,543-190,088,575 DUX4L6, RARRES2P4, 13 more genes
    nsv4597171copy number variation1nstd183human GRCh37 chr4: 190,890,428-191,027,923 , GRCh38.p12 chr4|NT_187650.1: 306,804-378,547 , GRCh38.p12 chr4: 189,969,273-190,106,768 RNA5SP174, FRG2, 17 more genes
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