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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
    nsv7057432inversion1nstd229human GRCh38 chr4: 4,018,387-9,499,063 , GRCh37.p13 chr4: 4,020,114-9,500,707 CPZ, OR7E85P, 127 more genes
    nsv7057425inversion1nstd229human GRCh38 chr4: 3,715,710-4,814,110 , GRCh37.p13 chr4: 3,717,437-4,815,837 UNC93B4, STX18, 30 more genes
    nsv7056110inversion1nstd229human GRCh38 chr4: 3,991,106-9,653,685 , GRCh37.p13 chr4: 3,992,833-9,655,309 MAN2B2, SH3TC1, 134 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
    nsv7044696inversion1nstd229human GRCh38 chr4: 3,996,444-9,648,382 , GRCh37.p13 chr4: 3,998,171-9,650,006 EVC, USP17L18, 134 more genes
    nsv7043983inversion1nstd229human GRCh38 chr4: 4,028,066-4,296,505 , GRCh37.p13 chr4: 4,029,793-4,298,232 UNC93B4, LOC107986252, 10 more genes
    nsv7039148inversion1nstd229human GRCh38 chr4: 4,150,240-8,956,846 , GRCh37.p13 chr4: 4,151,967-8,958,572 PPP2R2C, CRMP1, 80 more genes
    nsv7038223inversion1nstd229human GRCh38 chr4: 3,989,150-9,655,696 , GRCh37.p13 chr4: 3,990,877-9,657,320 RNA5SP152, MRFAP1, 134 more genes
    nsv6738071copy number variation1nstd229human GRCh38 chr4: 4,163,588-4,226,608 , GRCh37.p13 chr4: 4,165,315-4,228,335 OR7E43P, OTOP1
    nsv6737022copy number variation1nstd229human GRCh38 chr4: 4,223,607-4,232,434 , GRCh37.p13 chr4: 4,225,334-4,234,161 OTOP1
    nsv6736253copy number variation1nstd229human GRCh38 chr4: 4,205,330-4,205,594 , GRCh37.p13 chr4: 4,207,057-4,207,321 OTOP1
    nsv6736166copy number variation1nstd229human GRCh38 chr4: 3,268,098-4,744,559 , GRCh37.p13 chr4: 3,269,825-4,746,286 LOC105374355, LOC105374358, 40 more genes
    nsv6735580copy number variation1nstd229human GRCh38 chr4: 4,200,317-4,202,405 , GRCh37.p13 chr4: 4,202,044-4,204,132 OTOP1
    nsv6735270copy number variation1nstd229human GRCh38 chr4: 4,191,512-4,197,264 , GRCh37.p13 chr4: 4,193,239-4,198,991 OTOP1
    nsv6734339copy number variation1nstd229human GRCh38 chr4: 4,051,598-4,319,170 , GRCh37.p13 chr4: 4,053,325-4,320,897 OR7E43P, LYAR, 10 more genes
    nsv6734304copy number variation1nstd229human GRCh38 chr4: 4,219,744-4,258,931 , GRCh37.p13 chr4: 4,221,471-4,260,658 TMEM128, OTOP1
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