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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
    nsv7054202inversion1nstd229human GRCh38 chr4: 189,978,448-189,997,526 , GRCh37.p13 chr4: 190,899,603-190,918,681 , GRCh37.p13 chr4|NW_003571034.1: 71,378-90,456 TUBB7P
    nsv7039440inversion1nstd229human GRCh38 chr4: 189,981,347-189,986,989 , GRCh37.p13 chr4: 190,902,502-190,908,144 , GRCh37.p13 chr4|NW_003571034.1: 74,277-79,919 TUBB7P
    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
    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
    nsv6629666copy number variation1nstd224human GRCh37 chr4: 190,892,397-190,937,862 , GRCh38.p12 chr4: 189,971,242-190,016,707 RNA5SP174, TUBB7P, 2 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
    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
    nsv6629416copy number variation1nstd224human GRCh37 chr4: 189,401,460-190,915,650 , GRCh38.p12 chr4: 188,480,306-189,994,495 TUBB7P, FRG1-DT, 19 more genes
    nsv6315348copy number variation1nstd102humanPathogenic GRCh37 chr4: 174,944,132-190,957,473 , GRCh38.p12 chr4: 174,022,981-190,036,318 SPATA4, ADAM20P2, 203 more genes
    nsv6315316copy number variation1nstd102humanLikely pathogenic GRCh38 chr4: 186,194,495-190,175,048 , GRCh37.p13 chr4: 187,115,649-190,828,225 F11, FAT1, 74 more genes
    nsv6313744copy number variation1nstd102humanPathogenic GRCh37 chr4: 183,221,828-190,957,473 , GRCh38.p12 chr4: 182,300,675-190,036,318 RNU6-1053P, LINC02436, 141 more genes
    nsv6313663copy number variation1nstd102humanPathogenic GRCh37 chr4: 175,855,408-190,957,473 , GRCh38.p12 chr4: 174,934,257-190,036,318 LINC01596, NDUFB5P1, 190 more genes
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