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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141369insertion1nstd232human GRCh37.p13 chr16: 58,199,611-58,199,611 , GRCh38.p12 chr16: 58,165,707-58,165,707 CSNK2A2
    nsv7095031copy number variation2nstd102humanPathogenic GRCh37 chr16: 56,226,148-58,768,132 , GRCh38.p12 chr16: 56,192,236-58,734,228 MT1B, LOC105371293, 92 more genes
    nsv7094589copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,016,057-58,768,132 , GRCh38.p12 chr16: 56,982,145-58,734,228 SLC38A7, SETD6, 58 more genes
    nsv7069876inversion1nstd229human GRCh38 chr16: 58,076,774-64,694,512 , GRCh37.p13 chr16: 58,110,678-64,728,415 RN7SKP76, LOC105371311, 57 more genes
    nsv6992394copy number variation1nstd229human GRCh38 chr16: 58,170,101-58,172,200 , GRCh37.p13 chr16: 58,204,005-58,206,104 CSNK2A2
    nsv6990074copy number variation1nstd229human GRCh38 chr16: 58,170,501-58,172,200 , GRCh37.p13 chr16: 58,204,405-58,206,104 CSNK2A2
    nsv6985643copy number variation1nstd229human GRCh38 chr16: 58,174,881-58,175,294 , GRCh37.p13 chr16: 58,208,785-58,209,198 CSNK2A2
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6623239copy number variation1nstd224human GRCh37 chr16: 58,181,564-58,205,110 , GRCh38.p12 chr16: 58,147,660-58,171,206 CSNK2A2, LOC101927556
    nsv6590783inversion1nstd223human GRCh38 chr16: 58,169,051-58,169,555 , GRCh37.p13 chr16: 58,202,955-58,203,459 CSNK2A2
    nsv6582671inversion1nstd223human GRCh38 chr16: 58,171,518-58,171,873 , GRCh37.p13 chr16: 58,205,422-58,205,777 CSNK2A2
    nsv6582467inversion1nstd223human GRCh38 chr16: 58,178,604-58,179,163 , GRCh37.p13 chr16: 58,212,508-58,213,067 CSNK2A2
    nsv6513568copy number variation1nstd223human GRCh38 chr16: 58,169,201-58,171,000 , GRCh37.p13 chr16: 58,203,105-58,204,904 CSNK2A2
    nsv6510550copy number variation1nstd223human GRCh38 chr16: 58,151,903-58,156,314 , GRCh37.p13 chr16: 58,185,807-58,190,218 LOC101927556, CSNK2A2
    nsv6503972copy number variation1nstd223human GRCh38 chr16: 58,174,881-58,175,294 , GRCh37.p13 chr16: 58,208,785-58,209,198 CSNK2A2
    nsv6500313copy number variation1nstd223human GRCh38 chr16: 58,170,117-58,172,238 , GRCh37.p13 chr16: 58,204,021-58,206,142 CSNK2A2
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv6100296insertion1nstd212human GRCh38 chr16: 58,171,979-58,171,979 , GRCh37.p13 chr16: 58,205,883-58,205,883 CSNK2A2
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