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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3168066copy number variation1nstd158human GRCh37 chr5: 1,253,503-1,295,494 , GRCh38.p12 chr5: 1,253,388-1,295,379 TERT
    nsv3168635copy number variation1nstd158human GRCh37 chr3: 21,695,693-21,705,414 , GRCh38.p12 chr3: 21,654,201-21,663,922 ZNF385D
    nsv3169078copy number variation1nstd158human GRCh37 chr10: 19,462,244-19,464,396 , GRCh38.p12 chr10: 19,173,315-19,175,467 MALRD1
    nsv3168683copy number variation1nstd158human GRCh37 chr19: 32,462,002-32,463,796 , GRCh38.p12 chr19: 31,971,096-31,972,890 LINC01837
    nsv3168511copy number variation1nstd158human GRCh37 chr1: 110,792,717-110,793,901 , GRCh38.p12 chr1: 110,250,095-110,251,279 KCNC4
    nsv3168029copy number variation1nstd158human GRCh37 chr18: 40,417,995-40,418,946 , GRCh38.p12 chr18: 42,838,030-42,838,981 RIT2
    nsv3168125copy number variation1nstd158human GRCh37 chr11: 103,254,525-103,255,470 , GRCh38.p12 chr11: 103,383,797-103,384,742 DYNC2H1
    nsv3168580copy number variation1nstd158human GRCh37 chr16: 67,921,958-67,922,802 , GRCh38.p12 chr16: 67,888,055-67,888,899 NRN1L
    nsv3168191copy number variation1nstd158human GRCh37 chr9: 17,626,145-17,626,853 , GRCh38.p12 chr9: 17,626,147-17,626,855 SH3GL2
    nsv3168647copy number variation1nstd158human GRCh37 chr12: 41,876,220-41,876,885 , GRCh38.p12 chr12: 41,482,418-41,483,083 PDZRN4
    nsv3169186copy number variation1nstd158human GRCh37 chr1: 21,898,570-21,899,212 , GRCh38.p12 chr1: 21,572,077-21,572,719 ALPL
    nsv3169090copy number variation1nstd158human GRCh37 chr1: 213,319,631-213,320,431 , GRCh38.p12 chr1: 213,146,288-213,147,088 RPS6KC1
    nsv3167931copy number variation1nstd158human GRCh38.p12 chr1: 110,249,473-110,251,214 , GRCh37 chr1: 110,792,095-110,793,836 KCNC4
    nsv3169249inversion1nstd158human GRCh37 chr10: 13,267,786-13,279,885 , GRCh38.p12 chr10: 13,225,786-13,237,885 UCMA
    nsv3168068translocation1nstd158human GRCh37 chr2: 171,800,367-171,800,383 , GRCh37 chr11: 118,815,114-118,815,130 , GRCh38.p12 chr11: 118,944,405-118,944,421 , GRCh38.p12 chr2: 170,943,857-170,943,873 GORASP2
    nsv3167994translocation1nstd158human GRCh37 chr1: 143,130,383-143,131,259 , GRCh37 chr9: 68,421,741-68,422,617 , GRCh38.p12 chr9: 63,826,007-63,826,883 , GRCh38.p12 chr1|NT_187361.1: 12,622-13,498 LOC105379854
    nsv3168773copy number variation1nstd158human GRCh38.p12 chr4: 90,147,186-90,385,335 , GRCh37 chr4: 91,068,337-91,306,486 CCSER1, RN7SKP248
    nsv3168309copy number variation1nstd158human GRCh38.p12 chr10: 13,935,546-14,041,988 , GRCh37 chr10: 13,977,546-14,083,987 FRMD4A, LOC105376425
    nsv3167840copy number variation1nstd158human GRCh37 chr7: 132,826,241-132,961,184 , GRCh38.p12 chr7: 133,141,482-133,276,429 EXOC4, ST13P7
    nsv3169117copy number variation1nstd158human GRCh38.p12 chr16: 67,884,369-67,888,897 , GRCh37 chr16: 67,918,272-67,922,800 EDC4, NRN1L
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