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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7050522inversion1nstd229human GRCh38 chr4: 4,174,346-12,367,773 , GRCh37.p13 chr4: 4,176,073-12,369,397 USP17L29, MIR4274, 165 more genes
    nsv7047771inversion1nstd229human GRCh38 chr4: 11,077,762-13,240,771 , GRCh37.p13 chr4: 11,079,386-13,242,395 LOC107986179, LOC105374489, 15 more genes
    nsv6737302copy number variation1nstd229human GRCh38 chr4: 12,233,389-12,233,573 , GRCh37.p13 chr4: 12,235,013-12,235,197 LINC02270
    nsv6736063copy number variation1nstd229human GRCh38 chr4: 12,232,746-12,235,184 , GRCh37.p13 chr4: 12,234,370-12,236,808 LINC02270
    nsv6735907copy number variation1nstd229human GRCh38 chr4: 12,242,444-12,242,689 , GRCh37.p13 chr4: 12,244,068-12,244,313 LINC02270
    nsv6735475copy number variation1nstd229human GRCh38 chr4: 12,156,701-12,271,100 , GRCh37.p13 chr4: 12,158,325-12,272,724 LINC02270
    nsv6732435copy number variation1nstd229human GRCh38 chr4: 10,863,010-12,561,796 , GRCh37.p13 chr4: 10,864,634-12,563,420 RNPS1P1, MIR12113, 12 more genes
    nsv6731312copy number variation1nstd229human GRCh38 chr4: 11,874,688-13,148,345 , GRCh37.p13 chr4: 11,876,312-13,149,969 LOC105374492, LOC107986179, 6 more genes
    nsv6730956copy number variation1nstd229human GRCh38 chr4: 12,139,144-12,383,900 , GRCh37.p13 chr4: 12,140,768-12,385,524 LINC02270, RNU6-578P
    nsv6730911copy number variation1nstd229human GRCh38 chr4: 12,160,901-12,223,600 , GRCh37.p13 chr4: 12,162,525-12,225,224 LINC02270
    nsv6730266copy number variation1nstd229human GRCh38 chr4: 11,584,151-13,998,677 , GRCh37.p13 chr4: 11,585,775-14,000,301 LINC02270, LINC02360, 24 more genes
    nsv6727550copy number variation1nstd229human GRCh38 chr4: 12,159,701-12,223,400 , GRCh37.p13 chr4: 12,161,325-12,225,024 LINC02270
    nsv6726523copy number variation1nstd229human GRCh38 chr4: 12,205,101-12,227,800 , GRCh37.p13 chr4: 12,206,725-12,229,424 LINC02270
    nsv6724448copy number variation1nstd229human GRCh38 chr4: 10,838,974-12,561,796 , GRCh37.p13 chr4: 10,840,598-12,563,420 RNU6-578P, LOC105374490, 12 more genes
    nsv6723817copy number variation1nstd229human GRCh38 chr4: 12,156,785-12,271,130 , GRCh37.p13 chr4: 12,158,409-12,272,754 LINC02270
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