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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4681485copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 55,515,327-55,516,985 , GRCh38 chr16: 55,481,415-55,483,073 MMP2
    nsv4511372mobile element insertion1nstd166human GRCh37.p13 chr16: 55,525,340-55,525,340 , GRCh38.p12 chr16: 55,491,428-55,491,428 MMP2
    nsv4507301mobile element insertion1nstd166human GRCh37.p13 chr16: 55,536,242-55,536,242 , GRCh38.p12 chr16: 55,502,330-55,502,330 MMP2
    nsv4456077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,455,650-64,006,604 , GRCh38.p12 chr16: 53,421,738-63,972,700 MT1DP, RPL23AP91, 167 more genes
    nsv4365843copy number variation1nstd173human GRCh37 chr16: 46,464,489-55,795,214 , GRCh38.p12 chr16: 46,430,577-55,761,302 , LOC100526838, 158 more genes
    nsv4365186copy number variation1nstd173human GRCh37 chr16: 46,503,205-57,376,253 , GRCh38.p12 chr16: 46,469,293-57,342,341 , TOX3, 210 more genes
    nsv4250963copy number variation1nstd166human GRCh37.p13 chr16: 55,538,409-55,538,462 , GRCh38.p12 chr16: 55,504,497-55,504,550 MMP2
    nsv4238062copy number variation1nstd166human GRCh37.p13 chr16: 55,530,154-55,530,223 , GRCh38.p12 chr16: 55,496,242-55,496,311 MMP2
    nsv3961706insertion1nstd168human GRCh38 chr16: 55,485,845-55,537,608 , GRCh37.p13 chr16: 55,519,757-55,571,520 MMP2, LPCAT2
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
    nsv3918594copy number variation1nstd102humanPathogenic GRCh38 chr16: 50,784,329-55,566,715 , NCBI36 chr16: 49,375,741-54,158,128 , GRCh37 chr16: 50,818,240-55,600,627 TOX3, CASC22, 74 more genes
    nsv3918521copy number variation1nstd102humanPathogenic NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712 CYLD-AS2, MT1F, 342 more genes
    nsv3917427copy number variation1nstd102humanBenign NCBI36 chr16: 32,529,496-88,822,254 , GRCh37.p13 chr16: 32,621,995-90,294,753 , GRCh38.p12 chr16: 32,610,674-90,228,345 TXNL4B, KLHL36, 968 more genes
    nsv3916905copy number variation1nstd102humanBenign NCBI36 chr16: 32,481,314-88,822,254 , GRCh37.p13 chr16: 32,573,813-90,294,753 , GRCh38.p12 chr16: 32,562,492-90,228,345 CDH16, TP53TG3HP, 968 more genes
    nsv3916542copy number variation1nstd102humanPathogenic GRCh38 chr16: 55,457,477-63,841,622 , NCBI36 chr16: 54,048,890-62,433,027 , GRCh37 chr16: 55,491,389-63,875,526 CES1, SNORA46, 139 more genes
    nsv3915506copy number variation1nstd102humanPathogenic NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062 CFAP69P1, GAS8-AS1, 716 more genes
    nsv3915341copy number variation1nstd102humanBenign NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 GINS3, LINC00919, 985 more genes
    nsv3915118copy number variation1nstd102humanBenign NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 ZFHX3, CENPN-AS1, 985 more genes
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