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Items: 1 to 20 of 90

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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
    nsv5004049copy number variation1nstd200human GRCh38 chr16: 49,516,797-49,520,593 , GRCh37.p13 chr16: 49,550,708-49,554,504 ZNF423, ADAM3B
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4680405copy number variation1nstd189human GRCh37.p13 chr16: 49,422,792-49,644,803 , GRCh38.p12 chr16: 49,388,881-49,610,892 , ADAM3B, 4 more genes
    nsv4675028copy number variation1nstd102humanUncertain significance GRCh37 chr16: 49,469,515-49,961,548 , GRCh38.p12 chr16: 49,435,604-49,927,637 LOC105371244, MRPS21P8, 4 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
    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
    nsv3920484copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,466,829-51,673,196 , GRCh37 chr16: 46,500,741-51,707,107 , NCBI36 chr16: 45,058,242-50,264,608 NETO2, LOC100130180, 92 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
    nsv3916044copy number variation1nstd102humanPathogenic NCBI36 chr16: 45,058,242-50,947,206 , GRCh37 chr16: 46,500,741-52,389,705 , GRCh38 chr16: 46,466,829-52,355,793 LOC105371244, LOC105371241, 102 more genes
    nsv3915496copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,505,432-52,439,868 , GRCh38 chr16: 46,471,520-52,405,956 , NCBI36 chr16: 45,062,933-50,997,369 SNORD148, RN7SKP142, 102 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
    nsv3914752copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,500,741-51,973,216 , GRCh38 chr16: 46,466,829-51,939,304 , NCBI36 chr16: 45,058,242-50,530,717 CNEP1R1, RNU6-845P, 94 more genes
    nsv3912769copy number variation1nstd102humanBenign NCBI36 chr16: 31,862,658-88,822,254 , GRCh37.p13 chr16: 31,955,157-90,294,753 , GRCh38.p12 chr16: 31,943,836-90,228,345 MAF, LOC112268167, 985 more genes
    nsv3912665copy number variation1nstd102humanPathogenic NCBI36 chr16: 45,842,056-52,712,889 , GRCh37 chr16: 47,284,555-54,155,388 , GRCh38 chr16: 47,250,644-54,121,476 RPL10P14, ADCY7, 110 more genes
    nsv3912663copy 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 SMG1P7, LOC105371287, 985 more genes
    nsv3912156copy number variation1nstd102humanBenign NCBI36 chr16: 31,902,168-88,822,254 , GRCh37.p13 chr16: 31,994,667-90,294,753 , GRCh38.p12 chr16: 31,983,346-90,228,345 IST1, CMTR2, 985 more genes
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