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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6637194copy number variation1nstd102humanUncertain significance GRCh37 chr16: 20,631,242-20,784,335 , GRCh38.p12 chr16: 20,619,920-20,773,013 ACSM3, LOC100887080, 2 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 ACSM3, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 ACSM3, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 ACSM3, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 ACSM3, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 ACSM3, FTLP14, 1868 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 ACSM3, LOC105371069, 654 more genes
    nsv1398297copy number variation1nstd102humanPathogenic GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355 ACSM3, BMERB1, 701 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 ACSM3, NPIPB9, 597 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 ACSM3, 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 ACSM3, LOC729945, 450 more genes
    nsv3903116copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-22,442,007 , GRCh38.p12 chr16: 35,880-22,430,686 ACSM3, NPIPA8, 616 more genes
    nsv3917409copy number variation1nstd102humanPathogenic NCBI36 chr16: 14,956,252-28,225,665 , GRCh37 chr16: 15,048,751-28,318,164 , GRCh38 chr16: 14,954,894-28,306,843 ACSM3, SLC7A5P2, 251 more genes
    nsv3896782copy number variation1nstd102humanPathogenic GRCh37 chr16: 18,238,275-30,177,240 , GRCh38.p12 chr16: 18,144,418-30,165,919 ACSM3, SMG1P4, 287 more genes
    nsv3900243copy number variation1nstd102humanPathogenic GRCh37 chr16: 19,424,115-30,142,220 , GRCh38.p12 chr16: 19,412,793-30,130,899 ACSM3, RNU6-944P, 253 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ACSM3, ABAT, 876 more genes
    nsv4674963copy number variation1nstd102humanLikely benign GRCh37 chr16: 20,488,078-20,759,727 , GRCh38.p12 chr16: 20,476,756-20,748,405 ACSM3, ACSM1, 8 more genes
    nsv3912562copy number variation1nstd102humanUncertain significance GRCh37 chr16: 20,419,342-21,255,795 , GRCh38 chr16: 20,408,020-21,244,474 , NCBI36 chr16: 20,326,843-21,163,296 ACSM3, REXO5, 22 more genes
    nsv3895762copy number variation1nstd102humanUncertain significance GRCh37 chr16: 9,273,328-89,548,493 , GRCh38.p12 chr16: 9,179,471-89,482,085 ACSM3, HERC2P5, 1497 more genes
    nsv1398399copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,279,324-31,926,800 , GRCh38.p12 chr16: 1,229,323-31,915,479 ACSM3, FLYWCH2, 817 more genes
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