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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6992256copy number variation1nstd229human GRCh38 chr16: 47,725,786-49,432,895 , GRCh37.p13 chr16: 47,759,697-49,466,806 C16orf78, RNU6-257P, 24 more genes
    nsv6986915copy number variation1nstd229human GRCh38 chr16: 48,850,321-49,441,661 , GRCh37.p13 chr16: 48,884,232-49,475,572 LOC102724859, LOC102724847, 6 more genes
    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
    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
    nsv5940103copy number variation1nstd209human GRCh38 chr16: 49,281,573-49,281,779 , GRCh37.p13 chr16: 49,315,484-49,315,690 LOC102724859, CBLN1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 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
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