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Items: 1 to 20 of 207

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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
    nsv5941315copy number variation1nstd209human GRCh38 chr18: 49,046,088-49,046,302 , GRCh37.p13 chr18: 46,572,458-46,572,672 DYM, DYM-AS1
    nsv5322797copy number variation1nstd204human GRCh38.p13 chr18: 49,033,296-49,033,411 , GRCh37.p13 chr18: 46,559,666-46,559,781 DYM-AS1
    nsv5024189copy number variation1nstd200human GRCh38 chr18: 48,851,978-49,252,009 , GRCh37.p13 chr18: 46,378,349-46,778,379 LOC105372108, DYM-AS1, 4 more genes
    nsv5018004copy number variation1nstd200human GRCh38 chr18: 49,046,425-49,046,509 , GRCh37.p13 chr18: 46,572,795-46,572,879 DYM-AS1, DYM
    nsv5018003copy number variation1nstd200human GRCh38 chr18: 49,033,306-49,033,402 , GRCh37.p13 chr18: 46,559,676-46,559,772 DYM-AS1
    nsv4859580copy number variation1nstd200human GRCh37 chr18: 46,572,788-46,572,881 , GRCh38.p12 chr18: 49,046,418-49,046,511 DYM, DYM-AS1
    nsv4859579copy number variation1nstd200human GRCh37 chr18: 46,559,676-46,559,772 , GRCh38.p12 chr18: 49,033,306-49,033,402 DYM-AS1
    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
    nsv4532490copy number variation1nstd166human GRCh37.p13 chr18: 46,526,213-47,572,501 , GRCh38.p12 chr18: 48,999,843-50,046,131 , SNORD58A, 21 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
    nsv4457507copy number variation1nstd102humanUncertain significance GRCh37 chr18: 44,619,805-46,854,791 , GRCh38.p12 chr18: 47,093,434-49,328,421 LOC105372105, CTIF, 29 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
    nsv4271715copy number variation1nstd166human GRCh37.p13 chr18: 46,572,795-46,572,879 , GRCh38.p12 chr18: 49,046,425-49,046,509 DYM, DYM-AS1
    nsv4271134copy number variation1nstd166human GRCh37.p13 chr18: 46,559,676-46,559,772 , GRCh38.p12 chr18: 49,033,306-49,033,402 DYM-AS1
    nsv3962237copy number variation1nstd168human GRCh38 chr18: 49,039,008-49,054,097 , GRCh37.p13 chr18: 46,565,378-46,580,467 DYM, MIR4744, 1 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
    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
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