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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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 CBLN1, RPL10P14, 110 more genes
    nsv3910120copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,500,741-52,456,082 , NCBI36 chr16: 45,058,242-51,013,583 , GRCh38 chr16: 46,466,829-52,422,170 CBLN1, CYLD-AS1, 103 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 CBLN1, SNORD148, 102 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 CBLN1, CNEP1R1, 94 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 CBLN1, NETO2, 92 more genes
    nsv3903769copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,737,110-51,838,691 , GRCh38.p12 chr16: 46,703,198-51,804,780 CBLN1, N4BP1, 86 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 CBLN1, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 CBLN1, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 CBLN1, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 CBLN1, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 CBLN1, FTLP14, 1868 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 CBLN1, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 CBLN1, ATMIN, 826 more genes
    nsv3895555copy number variation1nstd102humanPathogenic GRCh37 chr16: 34,197,492-64,509,054 , GRCh38.p12 chr16: 34,963,121-64,475,151 CBLN1, RSPRY1, 362 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 CBLN1, LINC02140, 279 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CBLN1, CPNE2, 275 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 CBLN1, LOC105371244, 102 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 CBLN1, MAF, 985 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 CBLN1, GINS3, 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 CBLN1, ZFHX3, 985 more genes
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