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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3908109copy number variation1nstd102humanBenign GRCh37 chr16: 2,026,891-2,048,437 , GRCh38.p12 chr16: 1,976,890-1,998,436 SYNGR3, TBL3, 3 more genes
    nsv3900705copy number variation1nstd102humanBenign GRCh37 chr16: 2,026,891-2,043,980 , GRCh38.p12 chr16: 1,976,890-1,993,979 SYNGR3, NOXO1, 2 more genes
    nsv4455594copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-2,053,328 , GRCh38.p12 chr16: 35,880-2,003,327 SYNGR3, JPT2, 128 more genes
    nsv3919589copy number variation1nstd102humanPathogenic NCBI36 chr16: 36,766-1,987,584 , GRCh37 chr16: 96,766-2,047,583 , GRCh38 chr16: 46,766-1,997,582 SYNGR3, C1QTNF8, 127 more genes
    nsv4683390copy number variation1nstd102humanPathogenic GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004 SYNGR3, MRPS34, 102 more genes
    nsv4449893copy number variation1nstd102humanPathogenic GRCh37 chr16: 624,055-2,115,656 , GRCh38.p12 chr16: 574,055-2,065,655 SYNGR3, LMF1-AS1, 99 more genes
    nsv7098880copy number variation1nstd102humanPathogenic GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378 SYNGR3, TPSP1, 78 more genes
    nsv4683209copy number variation1nstd102humanPathogenic GRCh37 chr16: 1,203,718-2,185,710 , GRCh38.p12 chr16: 1,153,718-2,135,709 SYNGR3, TMEM204, 67 more genes
    nsv3893007copy number variation1nstd102humanPathogenic GRCh37 chr16: 1,734,363-2,285,561 , GRCh38.p12 chr16: 1,684,362-2,235,560 SYNGR3, IGFALS, 49 more genes
    nsv4682253copy number variation1nstd102humanPathogenic GRCh37 chr16: 1,573,499-2,114,448 , GRCh38.p12 chr16: 1,523,498-2,064,447 SYNGR3, NHERF2, 37 more genes
    nsv6637664copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,021,144-2,266,791 , GRCh38.p12 chr16: 1,971,143-2,216,790 SYNGR3, SNHG19, 22 more genes
    nsv6289860copy number variation1nstd102humanPathogenic GRCh38 chr16: 1,851,807-2,093,151 , GRCh37.p13 chr16: 1,901,808-2,143,152 SYNGR3, HS3ST6, 24 more genes
    nsv6315059copy number variation1nstd102humanPathogenic GRCh38 chr16: 1,903,155-2,093,402 , GRCh37.p13 chr16: 1,953,156-2,143,403 SYNGR3, NPW, 21 more genes
    nsv6637964copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,021,144-2,146,432 , GRCh38.p12 chr16: 1,971,143-2,096,431 SYNGR3, NTHL1, 11 more genes
    nsv6309997copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,003,468-2,126,543 , GRCh38.p12 chr16: 1,953,467-2,076,542 SYNGR3, NHERF2, 16 more genes
    nsv7094763copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,034,220-2,152,787 , GRCh38.p12 chr16: 1,984,219-2,102,786 SYNGR3, NHERF2, 10 more genes
    nsv6309998copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,034,220-2,136,892 , GRCh38.p12 chr16: 1,984,219-2,086,891 SYNGR3, GFER, 8 more genes
    nsv6310065copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,029,297-2,096,295 , GRCh38.p12 chr16: 1,979,296-2,046,294 SYNGR3, TSC2, 8 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 SYNGR3, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 SYNGR3, LOC100128079, 1879 more genes
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