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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5969313inversion1nstd209human GRCh38 chr18: 49,148,257-52,144,553 , GRCh37.p13 chr18: 46,674,627-49,670,923 , SMAD4, 52 more genes
    nsv5929106copy number variation1nstd209human GRCh38 chr18: 51,179,534-51,179,599 , GRCh37.p13 chr18: 48,705,904-48,705,969 MEX3C
    nsv5517695copy number variation1nstd206human GRCh38 chr18: 51,192,834-51,193,001 , GRCh37.p13 chr18: 48,719,204-48,719,371 , MEX3C
    nsv5151284mobile element insertion1nstd203human GRCh38 chr18: 51,193,530-51,193,536 , GRCh37.p13 chr18: 48,719,900-48,719,906 , MEX3C
    nsv5018066copy number variation1nstd200human GRCh38 chr18: 51,185,925-51,189,733 , GRCh37.p13 chr18: 48,712,295-48,716,103 MEX3C
    nsv5018065copy number variation1nstd200human GRCh38 chr18: 51,178,842-51,183,962 , GRCh37.p13 chr18: 48,705,212-48,710,332 MEX3C
    nsv5018064copy number variation1nstd200human GRCh38 chr18: 51,178,490-51,179,595 , GRCh37.p13 chr18: 48,704,860-48,705,965 MEX3C
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4629949copy number variation1nstd183human GRCh37 chr18: 48,701,388-48,701,534 , GRCh38.p12 chr18: 51,175,018-51,175,164 MEX3C
    nsv4499664mobile element insertion1nstd166human GRCh37.p13 chr18: 48,715,876-48,715,876 , GRCh38.p12 chr18: 51,189,506-51,189,506 MEX3C
    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
    nsv4264635copy number variation1nstd166human GRCh37.p13 chr18: 48,695,091-48,700,150 , GRCh38.p12 chr18: 51,168,721-51,173,780 MEX3C
    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
    nsv3923838copy number variation1nstd102humanPathogenic NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381 WDR7-OT1, HMGN1P30, 941 more genes
    nsv3921948copy number variation1nstd102humanPathogenic NCBI36 chr18: 34,628,690-61,451,020 , GRCh37 chr18: 36,374,692-63,300,040 , GRCh38 chr18: 38,794,728-65,632,804 HMGN1P30, LOC105372130, 314 more genes
    nsv3921745copy number variation1nstd102humanPathogenic GRCh38 chr18: 40,367,455-80,256,240 , NCBI36 chr18: 36,201,417-76,115,097 , GRCh37 chr18: 37,947,419-78,014,123 ARL2BPP1, LOC105372206, 448 more genes
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