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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314131copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202 COL20A1, HAR1A, 100 more genes
    nsv4676208copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,152,321-62,915,555 , GRCh38.p12 chr20: 62,555,114-64,284,202 COL20A1, GMEB2, 94 more genes
    nsv3916163copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,211,869-62,908,674 , GRCh38 chr20: 62,561,794-64,277,321 , NCBI36 chr20: 60,569,446-62,379,118 COL20A1, LOC105372727, 94 more genes
    nsv3916631copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,179,280-62,915,555 , NCBI36 chr20: 60,589,725-62,385,999 , GRCh38 chr20: 62,582,073-64,284,202 COL20A1, PTK6, 91 more genes
    nsv3922590copy number variation1nstd102humanPathogenic NCBI36 chr20: 60,553,022-62,343,283 , GRCh38 chr20: 62,545,370-64,241,486 , GRCh37 chr20: 61,142,577-62,872,839 COL20A1, RPL7P3, 95 more genes
    nsv3913089copy number variation1nstd102humanPathogenic NCBI36 chr20: 60,765,104-62,385,999 , GRCh37 chr20: 61,294,659-62,915,555 , GRCh38 chr20: 62,663,307-64,284,202 COL20A1, SLCO4A1-AS1, 89 more genes
    nsv3922908copy number variation1nstd102humanPathogenic NCBI36 chr20: 61,010,752-62,435,964 , GRCh37.p13 chr20: 61,540,307-62,965,520 , GRCh38.p12 chr20: 62,908,955-64,334,167 COL20A1, NPBWR2, 78 more genes
    nsv3911578copy number variation1nstd102humanPathogenic GRCh38 chr20: 62,455,231-63,839,491 , NCBI36 chr20: 60,463,682-61,941,288 , GRCh37 chr20: 61,030,287-62,470,844 COL20A1, LOC105372716, 70 more genes
    nsv6314091copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,619,222-62,915,555 , GRCh38.p12 chr20: 62,987,870-64,284,202 COL20A1, TPD52L2, 72 more genes
    nsv7148178copy number variation1nstd102humanPathogenic GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157 COL20A1, GID8, 60 more genes
    nsv6291738copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,775,756-62,915,555 , GRCh38.p12 chr20: 63,144,404-64,284,202 COL20A1, PTK6, 63 more genes
    nsv3911666copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,785,315-62,908,674 , GRCh38 chr20: 63,153,963-64,277,321 , NCBI36 chr20: 61,255,760-62,379,118 COL20A1, MIR3196, 63 more genes
    nsv3900085copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,827,144-62,907,526 , GRCh38.p12 chr20: 63,195,792-64,276,173 COL20A1, PCMTD2, 62 more genes
    nsv3909648copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,827,144-62,907,467 , GRCh38.p12 chr20: 63,195,792-64,276,114 COL20A1, LOC100130587, 62 more genes
    nsv3909335copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,884,113-62,915,555 , GRCh38.p12 chr20: 63,252,761-64,284,202 COL20A1, TCEA2, 59 more genes
    nsv3903709copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,429,900-62,293,991 , GRCh38.p12 chr20: 62,798,548-63,662,638 COL20A1, RNU6-994P, 48 more genes
    nsv3918154copy number variation1nstd102humanPathogenic NCBI36 chr20: 60,936,175-61,769,233 , GRCh37.p13 chr20: 61,465,730-62,298,789 , GRCh38.p12 chr20: 62,834,378-63,667,436 COL20A1, STMN3, 45 more genes
    nsv5381809copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,510,452-62,315,381 , GRCh38.p12 chr20: 62,879,100-63,684,028 COL20A1, MIR3196, 40 more genes
    nsv7095910copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,471,874-62,078,210 , GRCh38.p12 chr20: 62,840,522-63,446,857 COL20A1, LINC01749, 32 more genes
    nsv6314138copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,797,521-62,318,983 , GRCh38.p12 chr20: 63,166,169-63,687,630 COL20A1, HELZ2, 27 more genes
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