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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6968024copy number variation1nstd229human GRCh38 chr16: 631,153-633,052 , GRCh37.p13 chr16: 681,153-683,052 METTL26, WFIKKN1
    nsv6511799copy number variation1nstd223human GRCh38 chr16: 631,152-633,050 , GRCh37.p13 chr16: 681,152-683,050 METTL26, WFIKKN1
    nsv3895403copy number variation1nstd102humanBenign GRCh37 chr16: 682,670-685,708 , GRCh38.p12 chr16: 632,670-635,708 METTL26, WFIKKN1, 2 more genes
    nsv6196911copy number variation1nstd214human GRCh38 chr16: 635,397-635,464 , GRCh37.p13 chr16: 685,397-685,464 METTL26, TRG-CCC2-2, 1 more genes
    nsv6034622copy number variation1nstd212human GRCh38 chr16: 633,470-636,105 , GRCh37.p13 chr16: 683,470-686,105 METTL26, TRG-CCC2-2, 2 more genes
    nsv6027434copy number variation1nstd212human GRCh38 chr16: 635,419-635,486 , GRCh37.p13 chr16: 685,419-685,486 METTL26, TRG-CCC2-2, 1 more genes
    esv2750219copy number variation2estd201human GRCh37 chr16: 685,280-685,643 , GRCh38.p12 chr16: 635,280-635,643 METTL26, TRG-CCC2-2, 1 more genes
    esv3313467copy number variation1estd59human NCBI36 chr16: 621,052-625,850 , GRCh37.p13 chr16: 681,051-685,849 , GRCh38.p12 chr16: 631,051-635,849 METTL26, LOC100287175, 2 more genes
    esv3313466copy number variation51estd59human NCBI36 chr16: 621,052-625,850 , GRCh37.p13 chr16: 681,051-685,849 , GRCh38.p12 chr16: 631,051-635,849 METTL26, WFIKKN1, 2 more genes
    esv3402274copy number variation8estd59human NCBI36 chr16: 622,377-624,925 , GRCh37.p13 chr16: 682,376-684,924 , GRCh38.p12 chr16: 632,376-634,924 METTL26, WFIKKN1, 1 more genes
    nsv6976504copy number variation1nstd229human GRCh38 chr16: 599,402-638,384 , GRCh37.p13 chr16: 649,402-688,384 METTL26, TRG-CCC2-2, 3 more genes
    nsv6623477copy number variation1nstd224human GRCh37 chr16: 633,125-683,399 , GRCh38.p12 chr16: 583,125-633,399 METTL26, RAB40C, 2 more genes
    nsv6623481copy number variation2nstd224human GRCh37 chr16: 640,329-683,959 , GRCh38.p12 chr16: 590,329-633,959 METTL26, RAB40C, 1 more genes
    nsv5009322copy number variation1nstd200human GRCh38 chr16: 594,386-632,597 , GRCh37.p13 chr16: 644,386-682,597 METTL26, WFIKKN1, 2 more genes
    nsv943312copy number variation1nstd84human GRCh37 chr16: 668,202-684,117 , GRCh38.p12 chr16: 618,202-634,117 METTL26, RAB40C, 1 more genes
    nsv940182copy number variation1nstd84human GRCh37 chr16: 680,190-685,793 , GRCh38.p12 chr16: 630,190-635,793 METTL26, TRG-CCC2-2, 2 more genes
    nsv6089469insertion1nstd212human GRCh38 chr16: 635,517-635,517 , GRCh37.p13 chr16: 685,517-685,517 METTL26, TRG-CCC2-2, 1 more genes
    nsv4755264insertion1nstd199human GRCh38.p12 chr16: 635,430-635,430 , GRCh37 chr16: 685,430-685,430 METTL26, TRG-CCC2-2, 1 more genes
    nsv5652988insertion1nstd207human GRCh38 chr16: 635,397-635,397 , GRCh37.p13 chr16: 685,397-685,397 METTL26, TRG-CCC2-2, 1 more genes
    nsv3946640insertion1nstd167human GRCh38.p12 chr16: 635,397-635,397 , GRCh37 chr16: 685,397-685,397 METTL26, TRG-CCC2-2, 1 more genes
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