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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
    nsv7055239inversion1nstd229human GRCh38 chr4: 40,146,946-41,050,224 , GRCh37.p13 chr4: 40,148,566-41,052,241 RHOH, RBM47, 10 more genes
    nsv7051987inversion1nstd229human GRCh38 chr4: 40,180,050-40,693,331 , GRCh37.p13 chr4: 40,181,670-40,695,348 RBM47, RNU7-74P, 6 more genes
    nsv7049186inversion1nstd229human GRCh38 chr4: 38,135,041-40,245,309 , GRCh37.p13 chr4: 38,136,662-40,246,929 SMIM14, RNU6-887P, 42 more genes
    nsv7045186inversion1nstd229human GRCh38 chr4: 40,220,693-40,225,045 , GRCh37.p13 chr4: 40,222,313-40,226,665 RHOH
    nsv7038584inversion1nstd229human GRCh38 chr4: 38,474,718-40,416,508 , GRCh37.p13 chr4: 38,476,339-40,418,525 RPL9, UBE2K, 41 more genes
    nsv6737637copy number variation1nstd229human GRCh38 chr4: 40,245,208-40,416,509 , GRCh37.p13 chr4: 40,246,828-40,418,526 LINC02265, RHOH, 2 more genes
    nsv6735222copy number variation1nstd229human GRCh38 chr4: 40,234,438-40,307,497 , GRCh37.p13 chr4: 40,236,058-40,309,514 LINC02265, RHOH
    nsv6734514copy number variation1nstd229human GRCh38 chr4: 40,095,268-40,342,889 , GRCh37.p13 chr4: 40,096,888-40,344,906 LINC02265, CHRNA9, 2 more genes
    nsv6733906copy number variation1nstd229human GRCh38 chr4: 39,925,058-40,299,904 , GRCh37.p13 chr4: 39,926,678-40,301,921 N4BP2, RNU6-1112P, 6 more genes
    nsv6731359copy number variation1nstd229human GRCh38 chr4: 40,190,538-40,194,628 , GRCh37.p13 chr4: 40,192,158-40,196,248 RHOH
    nsv6730897copy number variation1nstd229human GRCh38 chr4: 40,244,343-40,250,643 , GRCh37.p13 chr4: 40,245,963-40,252,263 RHOH
    nsv6729219copy number variation1nstd229human GRCh38 chr4: 40,130,914-40,238,770 , GRCh37.p13 chr4: 40,132,534-40,240,390 RHOH, N4BP2
    nsv6726155copy number variation1nstd229human GRCh38 chr4: 39,630,360-40,250,301 , GRCh37.p13 chr4: 39,631,980-40,251,921 N4BP2, RNU6-1112P, 11 more genes
    nsv6722792copy number variation1nstd229human GRCh38 chr4: 39,797,627-40,362,367 , GRCh37.p13 chr4: 39,799,247-40,364,384 KRT18P25, PDS5A, 8 more genes
    nsv6721864copy number variation1nstd229human GRCh38 chr4: 40,245,110-40,247,931 , GRCh37.p13 chr4: 40,246,730-40,249,551 RHOH
    nsv6721628copy number variation1nstd229human GRCh38 chr4: 40,235,535-40,238,368 , GRCh37.p13 chr4: 40,237,155-40,239,988 RHOH
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
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