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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7054813inversion1nstd229human GRCh38 chr4: 189,637,195-189,942,235 , GRCh37.p13 chr4: 190,558,349-190,828,225 FRG1, LINC01596, 5 more genes
    nsv6774150copy number variation1nstd229human GRCh38 chr4: 189,894,093-189,961,631 , GRCh37.p13 chr4|NW_003571034.1: 1-54,561 FRG1-DT, FRG1
    nsv6770677copy number variation1nstd229human GRCh38 chr4: 189,931,901-189,971,400 , GRCh37.p13 chr4|NW_003571034.1: 24,831-64,330 FRG1-DT, FRG1
    nsv6762491copy number variation1nstd229human GRCh38 chr4: 189,963,315-189,982,340 , GRCh37.p13 chr4|NW_003571034.1: 56,245-75,270 MLLT10P2, FRG1, 1 more genes
    nsv6761641copy number variation1nstd229human GRCh38 chr4: 189,899,786-189,993,573 , GRCh37.p13 chr4|NW_003571034.1: 1-86,503 MLLT10P2, FRG1, 2 more genes
    nsv6760213copy number variation1nstd229human GRCh38 chr4: 189,893,046-189,963,889 , GRCh37.p13 chr4|NW_003571034.1: 1-56,819 FRG1-DT, FRG1
    nsv6760021copy number variation1nstd229human GRCh38 chr4: 189,660,843-189,994,352 , GRCh37.p13 chr4: 190,581,997-190,828,225 RNU1-51P, MLLT10P2, 7 more genes
    nsv6636995copy number variation1nstd102humanUncertain significance GRCh37 chr4: 187,853,428-190,957,473 , GRCh38.p12 chr4: 186,932,274-190,036,318 LINC02515, LINC02514, 49 more genes
    nsv6636301copy number variation1nstd102humanPathogenic GRCh37 chr4: 183,694,501-190,957,473 , GRCh38.p12 chr4: 182,773,348-190,036,318 LOC105377588, ENPP6, 139 more genes
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6634350copy number variation1nstd102humanPathogenic GRCh37 chr4: 185,211,271-190,957,473 , GRCh38.p12 chr4: 184,290,118-190,036,318 LINC02374, SLED1, 102 more genes
    nsv6629665copy number variation1nstd224human GRCh37 chr4: 190,864,510-190,937,862 , GRCh38.p12 chr4: 189,943,355-190,016,707 FRG1, RNA5SP174, 3 more genes
    nsv6629664copy number variation1nstd224human GRCh37 chr4: 190,758,884-190,915,650 , GRCh38.p12 chr4: 189,837,729-189,994,495 FRG1-DT, FRG1, 3 more genes
    nsv6629643copy number variation1nstd224human GRCh37 chr4: 186,873,844-190,872,778 , GRCh38.p12 chr4: 185,952,690-189,951,623 MTNR1A, TLR3, 61 more genes
    nsv6629607copy number variation1nstd224human GRCh37 chr4: 190,034,291-190,873,340 , GRCh38.p12 chr4: 189,113,137-189,952,185 HSP90AA4P, FRG1-DT, 9 more genes
    nsv6629471copy number variation2nstd224human GRCh37 chr4: 190,864,510-190,915,650 , GRCh38.p12 chr4: 189,943,355-189,994,495 TUBB7P, FRG1, 1 more genes
    nsv6629470copy number variation1nstd224human GRCh37 chr4: 190,758,884-190,880,409 , GRCh38.p12 chr4: 189,837,729-189,959,254 , GRCh38.p12 chr4|NT_187679.1: 486,458-555,799 , GRCh38.p12 chr4|NT_187543.1: 173,025-244,096 , GRCh38.p12 chr4|NT_187650.1: 172,562-296,785 FRG1, LINC01596, 1 more genes
    nsv6629421copy number variation1nstd224human GRCh37 chr4: 190,723,387-190,872,778 , GRCh38.p12 chr4: 189,802,233-189,951,623 , GRCh38.p12 chr4|NT_187679.1: 450,962-555,799 , GRCh38.p12 chr4|NT_187543.1: 135,786-244,096 , GRCh38.p12 chr4|NT_187650.1: 135,786-289,153 FRG1, LINC01596, 2 more genes
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