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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7145675copy number variation1nstd232human GRCh37.p13 chr4: 47,978,161-47,978,210 , GRCh38.p12 chr4: 47,976,144-47,976,193 CNGA1, LOC101927157
    nsv7048744inversion1nstd229human GRCh38 chr4: 47,920,338-48,060,660 , GRCh37.p13 chr4: 47,922,355-48,062,677 CNGA1, NIPAL1, 1 more genes
    nsv6735831copy number variation1nstd229human GRCh38 chr4: 47,965,887-47,965,940 , GRCh37.p13 chr4: 47,967,904-47,967,957 CNGA1, LOC101927157
    nsv6735578copy number variation1nstd229human GRCh38 chr4: 47,717,480-47,921,649 , GRCh37.p13 chr4: 47,719,497-47,923,666 LOC101927157, NFXL1, 2 more genes
    nsv6734946copy number variation1nstd229human GRCh38 chr4: 47,557,860-47,927,422 , GRCh37.p13 chr4: 47,559,877-47,929,439 RPL15P7, MIR8053, 6 more genes
    nsv6732666copy number variation1nstd229human GRCh38 chr4: 47,942,382-47,946,611 , GRCh37.p13 chr4: 47,944,399-47,948,628 CNGA1, LOC101927157
    nsv6729331copy number variation1nstd229human GRCh38 chr4: 47,925,764-47,933,910 , GRCh37.p13 chr4: 47,927,781-47,935,927 LOC101927157, CNGA1
    nsv6725734copy number variation1nstd229human GRCh38 chr4: 47,920,332-47,961,453 , GRCh37.p13 chr4: 47,922,349-47,963,470 LOC101927157, CNGA1
    nsv6724893copy number variation1nstd229human GRCh38 chr4: 47,989,675-47,990,055 , GRCh37.p13 chr4: 47,991,692-47,992,072 LOC101927157, CNGA1
    nsv6724033copy number variation1nstd229human GRCh38 chr4: 47,975,146-47,978,610 , GRCh37.p13 chr4: 47,977,163-47,980,627 CNGA1, LOC101927157
    nsv6722318copy number variation1nstd229human GRCh38 chr4: 47,850,478-48,000,485 , GRCh37.p13 chr4: 47,852,495-48,002,502 NFXL1, LOC101927157, 2 more genes
    nsv6719483copy number variation1nstd229human GRCh38 chr4: 47,921,973-47,931,555 , GRCh37.p13 chr4: 47,923,990-47,933,572 LOC101927157
    nsv6719397copy number variation1nstd229human GRCh38 chr4: 47,956,415-47,956,986 , GRCh37.p13 chr4: 47,958,432-47,959,003 LOC101927157, CNGA1
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6573114inversion1nstd223human GRCh38 chr4: 47,912,667-47,913,015 , GRCh37.p13 chr4: 47,914,684-47,915,032 LOC101927157, NFXL1
    nsv6571157inversion1nstd223human GRCh38 chr4: 47,957,171-47,957,534 , GRCh37.p13 chr4: 47,959,188-47,959,551 CNGA1, LOC101927157
    nsv6570647inversion1nstd223human GRCh38 chr4: 47,982,855-47,983,400 , GRCh37.p13 chr4: 47,984,872-47,985,417 CNGA1, LOC101927157
    nsv6566293inversion1nstd223human GRCh38 chr4: 47,979,039-47,980,515 , GRCh37.p13 chr4: 47,981,056-47,982,532 LOC101927157, CNGA1
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