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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7015620copy number variation1nstd229human GRCh38 chr18: 48,566,814-53,963,212 , GRCh37.p13 chr18: 46,093,185-51,489,582 LINC02837, RPL29P32, 65 more genes
    nsv7014223copy number variation1nstd229human GRCh38 chr18: 53,579,255-53,593,197 , GRCh37.p13 chr18: 51,105,625-51,119,567 LINC01919, LINC01917
    nsv7003631copy number variation1nstd229human GRCh38 chr18: 53,358,736-54,382,002 , GRCh37.p13 chr18: 50,885,106-51,908,372 POLI, MBD2, 7 more genes
    nsv6999423copy number variation1nstd229human GRCh38 chr18: 53,581,071-53,581,280 , GRCh37.p13 chr18: 51,107,441-51,107,650 LINC01917, LINC01919
    nsv6637893copy number variation1nstd102humanUncertain significance GRCh37 chr18: 48,273,185-51,134,173 , GRCh38.p12 chr18: 50,746,815-53,607,803 LOC105372121, LOC100420949, 23 more genes
    nsv6637509copy number variation1nstd102humanUncertain significance GRCh37 chr18: 49,666,138-51,804,494 , GRCh38.p12 chr18: 52,139,768-54,278,124 MIR4528, MBD2, 8 more genes
    nsv6624564copy number variation1nstd224human GRCh37 chr18: 51,055,233-51,448,811 , GRCh38.p12 chr18: 53,528,863-53,922,441 DCC, LINC01919, 2 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6314029copy number variation1nstd102humanPathogenic GRCh37 chr18: 50,707,829-54,924,248 , GRCh38.p12 chr18: 53,181,459-57,257,017 RNA5SP459, POLI, 42 more genes
    nsv6133450copy number variation1nstd213human GRCh37 chr18: 50,980,000-51,430,001 , GRCh38.p12 chr18: 53,453,630-53,903,631 DCC, RPL29P32, 2 more genes
    nsv6133333copy number variation1nstd213human GRCh37 chr18: 27,400,000-52,060,001 , GRCh38.p12 chr18: 29,820,035-54,532,766 ATP5F1A, DCC, 259 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv4676105copy number variation1nstd102humanPathogenic GRCh37 chr18: 49,460,596-78,014,123 , GRCh38.p12 chr18: 51,934,226-80,256,240 MIR548AV, GTSCR1, 310 more genes
    nsv4457866copy number variation1nstd102humanPathogenic GRCh37 chr18: 45,621,155-61,416,536 , GRCh38.p12 chr18: 48,094,784-63,749,302 LOC105372159, LOC105372156, 208 more genes
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4266432copy number variation1nstd166human GRCh37.p13 chr18: 51,026,225-52,514,743 , GRCh38.p12 chr18: 53,499,855-54,847,512 STARD6, DCC, 12 more genes
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 more genes
    nsv3924351copy number variation1nstd102humanPathogenic NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829 MIX23P1, LOC105372087, 942 more genes
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