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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 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
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv5321051copy number variation1nstd204human GRCh38.p13 chr18: 59,841,074-61,898,517 , GRCh37.p13 chr18: 57,508,306-59,565,750 LINC01544, LSM6P1, 28 more genes
    nsv5288436copy number variation1nstd204human GRCh37.p13 chr18: 57,702,833-58,277,033 , GRCh38.p13 chr18: 60,035,601-60,609,800 MC4R, LOC342784, 7 more genes
    nsv4881550inversion1nstd200human GRCh37 chr18: 57,639,759-62,087,901 , GRCh38.p12 chr18: 59,972,527-64,420,666 , RPL17P44, 59 more genes
    nsv4854731copy number variation1nstd200human GRCh37 chr18: 57,508,482-59,565,529 , GRCh38.p12 chr18: 59,841,250-61,898,296 RN7SL342P, RPS3AP49, 28 more genes
    nsv4704030copy number variation1nstd195human GRCh37 chr18: 57,973,251-58,097,651 , GRCh38.p12 chr18: 60,306,018-60,430,418 MC4R
    nsv4676378copy number variation1nstd102humanPathogenic GRCh37 chr18: 56,750,525-78,014,123 , GRCh38.p12 chr18: 59,083,293-80,256,240 HSBP1L1, TXNL4A, 231 more genes
    nsv4676158copy number variation1nstd102humanPathogenic GRCh37 chr18: 55,458,425-78,014,123 , GRCh38.p12 chr18: 57,791,193-80,256,240 LOC105372140, LOC105372143, 253 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
    nsv4436721copy number variation1nstd102humanPathogenic GRCh37 chr18: 57,940,764-58,095,560 , GRCh38.p12 chr18: 60,273,531-60,428,327 MC4R, LOC105372155
    nsv4346369copy number variation1nstd102humanPathogenic GRCh37 chr18: 58,024,137-77,996,821 , GRCh38.p12 chr18: 60,356,904-80,238,938 LOC105372221, LINC00683, 206 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
    nsv4261165copy number variation1nstd166human GRCh37.p13 chr18: 57,840,529-58,631,092 , GRCh38.p12 chr18: 60,173,296-60,963,859 HMGN1P31, LOC100421385, 8 more genes
    nsv4255192copy number variation1nstd166human GRCh37.p13 chr18: 57,525,880-58,308,922 , GRCh38.p12 chr18: 59,858,648-60,641,689 LOC101901828, LOC100421385, 16 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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