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Items: 1 to 20 of 49

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3910270copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141 XPO4, RNU6-71P, 1332 more genes
    nsv4675550copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-24,970,361 , GRCh38.p12 chr13: 18,862,146-24,396,223 XPO4, MRPL57, 129 more genes
    nsv3890184copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,008,480-25,534,121 , GRCh38.p12 chr13: 19,434,340-24,959,983 XPO4, ANKRD20A19P, 125 more genes
    nsv3912021copy number variation1nstd102humanPathogenic NCBI36 chr13: 19,144,074-24,458,010 , GRCh38 chr13: 19,671,934-24,985,872 , GRCh37 chr13: 20,246,074-25,560,010 XPO4, TPTE2P1, 119 more genes
    nsv4455063copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-23,274,540 , GRCh38.p12 chr13: 18,862,146-22,700,401 XPO4, SAP18, 90 more genes
    nsv6637646copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,287-22,089,005 , GRCh38.p12 chr13: 18,862,147-21,514,866 XPO4, LOC105370104, 78 more genes
    nsv4456640copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,562,171-22,993,375 , GRCh38.p12 chr13: 19,988,031-22,419,236 XPO4, RANP8, 53 more genes
    nsv3919995copy number variation1nstd102humanPathogenic NCBI36 chr13: 19,206,550-21,596,737 , GRCh37.p13 chr13: 20,308,550-22,698,737 , GRCh38.p12 chr13: 19,734,410-22,124,598 XPO4, IFT88, 56 more genes
    nsv4675255copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,668,070-23,029,230 , GRCh38.p12 chr13: 20,093,931-22,455,091 XPO4, RPSAP54, 52 more genes
    nsv3914641copy number variation1nstd102humanPathogenic GRCh38 chr13: 19,885,283-22,014,498 , NCBI36 chr13: 19,357,423-21,486,637 , GRCh37 chr13: 20,459,423-22,588,637 XPO4, LOC105370102, 49 more genes
    nsv3916109copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,600,790-22,541,928 , GRCh38 chr13: 20,026,650-21,967,789 , NCBI36 chr13: 19,498,790-21,439,928 XPO4, LOC105370103, 49 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 XPO4, RNU6-80P, 1334 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 XPO4, LINC00363, 1334 more genes
    nsv3897246copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,031,237-115,107,157 , GRCh38.p12 chr13: 18,457,097-114,341,682 XPO4, NT5CP3, 1334 more genes
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 XPO4, GRTP1, 1334 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 XPO4, RN7SL272P, 1333 more genes
    nsv3894298copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,058,717-115,103,529 , GRCh38.p12 chr13: 18,484,577-114,338,054 XPO4, DZIP1, 1333 more genes
    nsv3916629copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,139,188-115,085,141 , NCBI36 chr13: 18,037,188-114,110,750 , GRCh38 chr13: 18,565,048-114,327,173 XPO4, TM9SF2, 1330 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 XPO4, MTUS2-AS1, 1330 more genes
    nsv3914899copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-115,107,733 , GRCh38 chr13: 18,862,146-114,342,258 , NCBI36 chr13: 18,334,286-114,125,835 XPO4, EFNB2, 1319 more genes
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