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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6291811copy number variation1nstd102humanUncertain significance GRCh37 chr16: 12,007,434-12,085,776 , GRCh38.p12 chr16: 11,913,577-11,991,919 TNFRSF17, GSPT1, 3 more genes
    nsv6637966copy number variation1nstd102humanUncertain significance GRCh37 chr16: 12,007,435-12,073,710 , GRCh38.p12 chr16: 11,913,578-11,979,853 TNFRSF17, GSPT1, 3 more genes
    nsv3918732copy number variation1nstd102humanPathogenic GRCh37 chr16: 12,061,688-15,256,745 , GRCh38 chr16: 11,967,831-15,162,888 , NCBI36 chr16: 11,969,189-15,164,246 TNFRSF17, LOC105371087, 62 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 TNFRSF17, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 TNFRSF17, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 TNFRSF17, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 TNFRSF17, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 TNFRSF17, FTLP14, 1868 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 TNFRSF17, LOC105371069, 654 more genes
    nsv1398297copy number variation1nstd102humanPathogenic GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355 TNFRSF17, BMERB1, 701 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 TNFRSF17, NPIPB9, 597 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 TNFRSF17, MIR6511B2, 535 more genes
    nsv3910441copy number variation1nstd102humanPathogenic NCBI36 chr16: 4,634,894-29,089,642 , GRCh37 chr16: 4,694,893-29,182,141 , GRCh38 chr16: 4,644,892-29,170,820 TNFRSF17, LOC729945, 450 more genes
    nsv3903116copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-22,442,007 , GRCh38.p12 chr16: 35,880-22,430,686 TNFRSF17, NPIPA8, 616 more genes
    nsv3900978copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-19,806,921 , GRCh38.p12 chr16: 35,880-19,795,599 TNFRSF17, LOC105371091, 543 more genes
    nsv3915829copy number variation1nstd102humanPathogenic NCBI36 chr16: 656,663-15,744,462 , GRCh38 chr16: 666,662-15,743,104 , GRCh37 chr16: 716,662-15,836,961 TNFRSF17, RPL35AP34, 429 more genes
    nsv3923267copy number variation1nstd102humanPathogenic GRCh37 chr16: 93,732-13,420,663 , GRCh38 chr16: 43,732-13,326,806 , NCBI36 chr16: 33,732-13,328,164 TNFRSF17, METRN, 413 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 TNFRSF17, ABAT, 876 more genes
    nsv3917207copy number variation1nstd102humanLikely pathogenic NCBI36 chr16: 11,953,825-15,187,557 , GRCh37 chr16: 12,046,324-15,280,056 , GRCh38 chr16: 11,952,467-15,186,199 TNFRSF17, ERCC4, 63 more genes
    nsv3886214copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 11,369,400-13,577,493 , GRCh37.p13 chr16: 11,463,257-13,671,350 TNFRSF17, GSPT1, 30 more genes
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