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Items: 1 to 20 of 179

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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
    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
    nsv4531165copy number variation1nstd166human GRCh37.p13 chr18: 47,100,791-47,465,427 , GRCh38.p12 chr18: 49,574,421-49,939,057 , MYO5B, 7 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
    nsv4457865copy number variation1nstd102humanUncertain significance GRCh37 chr18: 47,103,259-47,463,796 , GRCh38.p12 chr18: 49,576,889-49,937,426 LOC105372112, LIPG, 6 more genes
    nsv4457585copy number variation1nstd102humanUncertain significance GRCh37 chr18: 47,097,488-47,470,054 , GRCh38.p12 chr18: 49,571,118-49,943,684 LOC105372112, SCARNA17, 6 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
    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
    nsv3920818copy number variation1nstd102humanPathogenic NCBI36 chr18: 15,370,696-76,117,153 , GRCh37.p13 chr18: 15,380,696-78,016,181 , GRCh38.p12 chr18: 15,380,697-80,258,298 AQP4-AS1, SERPINB8, 670 more genes
    nsv3919004copy number variation1nstd102humanPathogenic GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097 LIVAR, LINC03069, 941 more genes
    nsv3918642copy number variation1nstd102humanPathogenic GRCh38 chr18: 49,199,411-80,254,946 , NCBI36 chr18: 44,979,779-76,113,817 , GRCh37 chr18: 46,725,781-78,012,829 CDH19, NETO1-DT, 360 more genes
    nsv3918488copy number variation1nstd102humanPathogenic NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869 LOC105372027, ASXL3, 945 more genes
    nsv3916426copy number variation1nstd102humanPathogenic GRCh37 chr18: 149,089-77,992,274 , NCBI36 chr18: 139,089-76,093,265 , GRCh38 chr18: 149,089-80,234,391 TPGS2, TWSG1-DT, 941 more genes
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