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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv5501226copy number variation1nstd206human GRCh38 chr12: 1,823,146-1,823,289 , GRCh37.p13 chr12: 1,932,312-1,932,455 LRTM2, CACNA2D4
    nsv5277594copy number variation1nstd204human GRCh38.p13 chr12: 1,791,001-1,825,200 , GRCh37.p13 chr12: 1,900,167-1,934,366 CACNA2D4, LOC105369601, 2 more genes
    nsv4987981copy number variation1nstd200human GRCh38 chr12: 1,823,422-1,824,803 , GRCh37.p13 chr12: 1,932,588-1,933,969 LRTM2, CACNA2D4
    nsv4843721copy number variation1nstd200human GRCh37 chr12: 1,932,588-1,933,969 , GRCh38.p12 chr12|NW_018654718.1: 165,566-166,947 , GRCh38.p12 chr12: 1,823,422-1,824,803 CACNA2D4, LRTM2
    nsv4765521inversion1nstd199human GRCh37 chr12: 164,697-2,866,263 , GRCh38.p12 chr12: 55,531-2,757,097 , CACNA1C, 51 more genes
    nsv4729176copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,242-4,683,495 , GRCh38.p12 chr12: 82,076-4,574,329 RPL18P9, CACNA1C, 92 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4604376copy number variation2nstd183human GRCh37 chr12: 545,318-2,170,181 , GRCh38.p12 chr12: 436,152-2,061,015 , CCDC77, 31 more genes
    nsv4457052copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-6,346,092 , GRCh38.p12 chr12: 64,620-6,236,926 TSPAN9, RNU6-174P, 118 more genes
    nsv4456539copy number variation1nstd102humanUncertain significance GRCh37 chr12: 1,436,977-2,156,672 , GRCh38.p12 chr12|NW_018654718.1: 1-389,650 , GRCh38.p12 chr12: 1,327,811-2,047,506 CACNA1C, CACNA1C-IT2, 18 more genes
    nsv4456179copy number variation1nstd102humanUncertain significance GRCh37 chr12: 1,944,805-1,986,237 , GRCh38.p12 chr12|NW_018654718.1: 177,783-219,215 , GRCh38.p12 chr12: 1,835,639-1,877,071 LAMP1P1, CACNA2D4, 1 more genes
    nsv4455858copy number variation3nstd102humanUncertain significance GRCh37 chr12: 1,944,712-1,986,237 , GRCh38.p12 chr12|NW_018654718.1: 177,690-219,215 , GRCh38.p12 chr12: 1,835,546-1,877,071 CACNA2D4, LAMP1P1, 1 more genes
    nsv4455658copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-8,393,815 , GRCh38.p12 chr12: 64,620-8,241,219 PLEKHG6, MIR141, 226 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
    nsv4428932copy number variation1nstd174human GRCh37 chr12: 1,944,485-1,987,245 , GRCh38.p12 chr12: 1,835,319-1,878,079 , GRCh38.p12 chr12|NW_018654718.1: 177,463-220,223 LRTM2, LAMP1P1, 1 more genes
    nsv4383887copy number variation1nstd173human GRCh37 chr12: 1,944,713-1,985,286 , GRCh38.p12 chr12: 1,835,547-1,876,120 , GRCh38.p12 chr12|NW_018654718.1: 177,691-218,264 LRTM2, LAMP1P1, 1 more genes
    nsv4377959copy number variation1nstd173human GRCh37 chr12: 1,944,806-1,986,237 , GRCh38.p12 chr12: 1,835,640-1,877,071 , GRCh38.p12 chr12|NW_018654718.1: 177,784-219,215 LAMP1P1, LRTM2, 1 more genes
    nsv4371243copy number variation2nstd173human GRCh37 chr12: 1,944,713-1,986,237 , GRCh38.p12 chr12: 1,835,547-1,877,071 , GRCh38.p12 chr12|NW_018654718.1: 177,691-219,215 LRTM2, LAMP1P1, 1 more genes
    nsv4366864copy number variation1nstd173human GRCh37 chr12: 1,944,713-1,986,249 , GRCh38.p12 chr12: 1,835,547-1,877,083 , GRCh38.p12 chr12|NW_018654718.1: 177,691-219,227 CACNA2D4, LRTM2, 1 more genes
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