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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3921940copy number variation1nstd102humanLikely benign NCBI36 chr8: 56,826,229-57,012,361 , GRCh37 chr8: 56,663,675-56,849,807 , GRCh38 chr8: 55,751,116-55,937,248 TGS1, TMEM68, 2 more genes
    nsv3921418copy number variation1nstd102humanBenign GRCh37 chr8: 56,725,646-56,879,608 , NCBI36 chr8: 56,888,200-57,042,162 , GRCh38 chr8: 55,813,087-55,967,049 TGS1, SNORA1B, 1 more genes
    nsv3904683copy number variation1nstd102humanBenign GRCh37 chr8: 56,722,691-56,874,017 , GRCh38.p12 chr8: 55,810,132-55,961,458 TGS1, LYN, 1 more genes
    nsv4674115copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,653,722-234,591,807 , GRCh38.p12 chr1: 223,480,380-234,456,061 LOC105373163, CDC42BPA, 258 more genes
    nsv3893439copy number variation1nstd102humanPathogenic GRCh37 chr8: 49,822,483-58,822,602 , GRCh38.p12 chr8: 48,909,924-57,910,043 TGS1, SEPTIN10P1, 110 more genes
    nsv3911944copy number variation1nstd102humanPathogenic GRCh37 chr8: 54,237,949-62,775,577 , GRCh38 chr8: 53,325,389-61,863,018 , NCBI36 chr8: 54,400,502-62,938,131 TGS1, SOX17, 119 more genes
    nsv3924755copy number variation1nstd102humanPathogenic NCBI36 chr8: 50,546,890-58,900,583 , GRCh37 chr8: 50,384,337-58,738,029 , GRCh38 chr8: 49,471,778-57,825,470 TGS1, LOC105375849, 103 more genes
    nsv3899452copy number variation1nstd102humanPathogenic NCBI36 chr1: 224,439,448-231,074,857 , GRCh37 chr1: 226,372,825-233,008,234 , GRCh38 chr1: 226,185,124-232,872,488 RNA5S10, SIPA1L2, 178 more genes
    nsv3923501copy number variation1nstd102humanPathogenic NCBI36 chr8: 55,896,471-62,221,415 , GRCh38 chr8: 54,821,357-61,146,302 , GRCh37 chr8: 55,733,917-62,058,861 TGS1, NUDT15P1, 83 more genes
    nsv4674157copy number variation1nstd102humanPathogenic GRCh37 chr1: 222,641,389-228,137,574 , GRCh38.p12 chr1: 222,468,047-227,949,873 SRP9, AKR1B1P1, 123 more genes
    nsv3908695copy number variation1nstd102humanPathogenic NCBI36 chr1: 221,587,658-226,810,656 , GRCh38 chr1: 223,347,693-228,556,332 , GRCh37 chr1: 223,521,035-228,744,033 SNAP47, OBSCN-AS1, 137 more genes
    nsv3899116copy number variation1nstd102humanPathogenic NCBI36 chr1: 223,636,497-228,621,170 , GRCh38 chr1: 225,382,172-230,418,801 , GRCh37 chr1: 225,569,874-230,554,547 ISCA1P2, TUBB8P10, 146 more genes
    nsv3919070copy number variation1nstd102humanPathogenic NCBI36 chr8: 54,569,654-58,566,126 , GRCh37.p13 chr8: 54,407,101-58,403,572 , GRCh38.p12 chr8: 53,494,541-57,491,013 TGS1, BPNT2, 73 more genes
    nsv3919101copy number variation1nstd102humanPathogenic GRCh38 chr8: 55,423,413-58,836,753 , NCBI36 chr8: 56,498,527-59,911,866 , GRCh37 chr8: 56,335,973-59,749,312 TGS1, RPL37P6, 59 more genes
    nsv3912773copy number variation1nstd102humanPathogenic GRCh37 chr8: 55,677,510-57,697,858 , NCBI36 chr8: 55,840,064-57,860,412 , GRCh38 chr8: 54,764,950-56,785,299 TGS1, MOS, 36 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 MARK1, LINC02766, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 SNAP47, STK40, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 RNU1-153P, MIR3917, 4887 more genes
    nsv3915173copy number variation1nstd102humanPathogenic NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636 TGS1, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 TGS1, TBC1D31, 2109 more genes
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