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Items: 1 to 20 of 291

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5532539copy number variation1nstd206human GRCh38 chr16: 4,967,648-4,968,067 , GRCh37.p13 chr16: 5,017,649-5,018,068 SEC14L5
    nsv5529697copy number variation1nstd206human GRCh38 chr16: 4,957,857-5,308,524 , GRCh37.p13 chr16: 5,007,858-5,358,525 , LOC105371067, 12 more genes
    nsv5527611copy number variation1nstd206human GRCh38 chr16: 5,004,687-5,310,668 , GRCh37.p13 chr16: 5,054,688-5,360,669 , RPS3AP48, 12 more genes
    nsv5523082copy number variation1nstd206human GRCh38 chr16: 4,966,021-4,968,338 , GRCh37.p13 chr16: 5,016,022-5,018,339 SEC14L5
    nsv5519557copy number variation1nstd206human GRCh38 chr16: 4,998,000-4,999,504 , GRCh37.p13 chr16: 5,048,001-5,049,505 SEC14L5
    nsv5518574copy number variation1nstd206human GRCh38 chr16: 4,978,133-4,978,433 , GRCh37.p13 chr16: 5,028,134-5,028,434 SEC14L5
    nsv5349443translocation1nstd200human GRCh38 chr16: 5,007,606-5,007,606 , GRCh38 chr16: 5,008,155-5,008,155 , GRCh37.p13 chr16: 5,057,607-5,057,607 , GRCh37.p13 chr16: 5,058,156-5,058,156 SEC14L5
    nsv5349442translocation1nstd200human GRCh38 chr16: 5,000,090-5,000,090 , GRCh38 chr16: 4,999,900-4,999,900 , GRCh37.p13 chr16: 5,049,901-5,049,901 , GRCh37.p13 chr16: 5,050,091-5,050,091 SEC14L5
    nsv5313629copy number variation1nstd204human GRCh38.p13 chr16: 4,957,847-5,308,533 , GRCh37.p13 chr16: 5,007,848-5,358,534 , SEC14L5, 12 more genes
    nsv5271132copy number variation1nstd204human GRCh38.p13 chr16: 4,956,780-4,982,728 , GRCh37.p13 chr16: 5,006,781-5,032,729 SEC14L5
    nsv5269327copy number variation1nstd204human GRCh37.p13 chr16: 5,008,302-5,252,801 , GRCh38.p13 chr16: 4,958,301-5,202,800 SEC14L5, NAGPA, 6 more genes
    nsv5264148copy number variation1nstd204human GRCh38.p13 chr16: 4,977,957-4,998,129 , GRCh37.p13 chr16: 5,027,958-5,048,130 SEC14L5
    nsv5181736mobile element insertion1nstd203human GRCh38 chr16: 5,014,708-5,014,713 , GRCh37.p13 chr16: 5,064,709-5,064,714 SEC14L5
    nsv5144662mobile element insertion1nstd203human GRCh38 chr16: 4,977,446-4,977,480 , GRCh37.p13 chr16: 5,027,447-5,027,481 SEC14L5
    nsv5008134copy number variation1nstd200human GRCh38 chr16: 5,000,270-5,002,527 , GRCh37.p13 chr16: 5,050,271-5,052,528 SEC14L5
    nsv5008133copy number variation1nstd200human GRCh38 chr16: 4,980,749-4,981,379 , GRCh37.p13 chr16: 5,030,750-5,031,380 SEC14L5
    nsv5008132copy number variation1nstd200human GRCh38 chr16: 4,978,737-4,981,202 , GRCh37.p13 chr16: 5,028,738-5,031,203 SEC14L5
    nsv5008131copy number variation1nstd200human GRCh38 chr16: 4,973,960-4,978,836 , GRCh37.p13 chr16: 5,023,961-5,028,837 SEC14L5
    nsv5008130copy number variation1nstd200human GRCh38 chr16: 4,966,021-4,968,338 , GRCh37.p13 chr16: 5,016,022-5,018,339 SEC14L5
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