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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7074500inversion1nstd229human GRCh38 chr16: 57,094,373-57,125,844 , GRCh37.p13 chr16: 57,128,285-57,159,756 CPNE2
    nsv7062252inversion1nstd229human GRCh38 chr16: 57,095,623-57,128,596 , GRCh37.p13 chr16: 57,129,535-57,162,508 CPNE2
    nsv7059832inversion1nstd229human GRCh38 chr16: 57,121,586-57,121,700 , GRCh37.p13 chr16: 57,155,498-57,155,612 CPNE2
    nsv6997325copy number variation1nstd229human GRCh38 chr16: 57,129,604-57,132,444 , GRCh37.p13 chr16: 57,163,516-57,166,356 CPNE2
    nsv6986991copy number variation1nstd229human GRCh38 chr16: 57,059,649-57,664,041 , GRCh37.p13 chr16: 57,093,561-57,697,953 CPNE2, TRL-CAG2-1, 21 more genes
    nsv6986615copy number variation1nstd229human GRCh38 chr16: 57,106,612-57,106,699 , GRCh37.p13 chr16: 57,140,524-57,140,611 CPNE2
    nsv6983715copy number variation1nstd229human GRCh38 chr16: 57,147,183-57,147,520 , GRCh37.p13 chr16: 57,181,095-57,181,432 CPNE2
    nsv6983224copy number variation1nstd229human GRCh38 chr16: 57,103,623-57,108,972 , GRCh37.p13 chr16: 57,137,535-57,142,884 CPNE2
    nsv6982873copy number variation1nstd229human GRCh38 chr16: 57,098,623-57,103,739 , GRCh37.p13 chr16: 57,132,535-57,137,651 CPNE2
    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
    nsv6510045copy number variation1nstd223human GRCh38 chr16: 57,138,565-57,140,106 , GRCh37.p13 chr16: 57,172,477-57,174,018 CPNE2
    nsv6503379copy number variation1nstd223human GRCh38 chr16: 57,106,611-57,106,699 , GRCh37.p13 chr16: 57,140,523-57,140,611 CPNE2
    nsv6501037copy number variation1nstd223human GRCh38 chr16: 57,132,898-57,133,355 , GRCh37.p13 chr16: 57,166,810-57,167,267 CPNE2
    nsv6315060copy number variation1nstd102humanPathogenic GRCh38 chr16: 53,818,483-57,631,312 , GRCh37.p13 chr16: 53,852,395-57,665,224 LOC105371283, MT1A, 91 more genes
    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
    nsv6274074copy number variation1nstd214human GRCh38 chr16: 57,106,611-57,106,698 , GRCh37.p13 chr16: 57,140,523-57,140,610 CPNE2
    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
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