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Items: 1 to 20 of 38

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7136984copy number variation1nstd102humanUncertain significance GRCh37 chr16: 46,940,888-46,965,210 , GRCh38.p12 chr16: 46,906,976-46,931,298 GPT2
    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 GPT2, 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 GPT2, 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 GPT2, 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 GPT2, NETO2, 92 more genes
    nsv3903769copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,737,110-51,838,691 , GRCh38.p12 chr16: 46,703,198-51,804,780 GPT2, N4BP1, 86 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 GPT2, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 GPT2, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 GPT2, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 GPT2, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 GPT2, 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 GPT2, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 GPT2, ATMIN, 826 more genes
    nsv3895555copy number variation1nstd102humanPathogenic GRCh37 chr16: 34,197,492-64,509,054 , GRCh38.p12 chr16: 34,963,121-64,475,151 GPT2, RSPRY1, 362 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 GPT2, LINC02140, 279 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 GPT2, 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 GPT2, 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 GPT2, 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 GPT2, 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 GPT2, ZFHX3, 985 more genes
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