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Items: 1 to 20 of 492

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097788copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,047,551-145,049,537 , GRCh38.p12 chr8: 143,973,383-143,975,369 PLEC, PARP10
    nsv6873776copy number variation1nstd229human GRCh38 chr8: 143,662,901-144,626,400 , GRCh37.p13 chr8: 145,146,063-145,851,785 LRRC14, SCX, 67 more genes
    nsv6866250copy number variation1nstd229human GRCh38 chr8: 143,771,901-144,562,100 , GRCh37.p13 chr8: 145,146,063-145,787,484 MIR939, MIR10400, 58 more genes
    nsv6859041copy number variation1nstd229human GRCh38 chr8: 143,981,273-143,981,389 , GRCh37.p13 chr8|NW_003315923.1: 319,918-320,034 , GRCh37.p13 chr8: 145,055,441-145,055,557 PARP10
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632684copy number variation3nstd224human GRCh37 chr8: 144,942,135-145,057,683 , GRCh38.p12 chr8: 143,867,967-143,983,515 PLEC, EPPK1, 2 more genes
    nsv6632571copy number variation1nstd224human GRCh37 chr8: 144,946,799-145,072,539 , GRCh38.p12 chr8: 143,872,631-143,998,371 PLEC, GRINA, 3 more genes
    nsv6558782inversion1nstd223human GRCh38 chr8: 143,001,224-145,028,420 , GRCh37.p13 chr8: 144,082,641-146,253,806 ZFP41, LY6H, 118 more genes
    nsv6430241copy number variation1nstd223human GRCh38 chr8: 143,844,521-144,567,758 , GRCh37.p13 chr8: 145,146,063-145,793,142 MFSD3, SLC39A4, 51 more genes
    nsv6426781copy number variation1nstd223human GRCh38 chr8: 143,707,640-143,976,091 , GRCh37.p13 chr8|NW_003315923.1: 46,285-314,736 , GRCh37.p13 chr8: 144,789,810-145,050,259 MIR661, LOC107986985, 15 more genes
    nsv6425791copy number variation1nstd223human GRCh38 chr8: 142,975,701-144,021,300 , GRCh37.p13 chr8: 144,057,118-144,743,525 LY6H, RHPN1-AS1, 55 more genes
    nsv6420919copy number variation1nstd223human GRCh38 chr8: 143,980,057-143,982,199 , GRCh37.p13 chr8: 145,054,225-145,056,367 , GRCh37.p13 chr8|NW_003315923.1: 318,702-320,844 PARP10
    nsv6417121copy number variation1nstd223human GRCh38 chr8: 143,683,447-144,365,810 , GRCh37.p13 chr8|NW_003315923.1: 22,092-429,806 , GRCh37.p13 chr8: 144,765,617-145,589,470 EPPK1, PARP10, 42 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313487copy number variation1nstd102humanPathogenic GRCh37 chr8: 130,863,093-146,295,771 , GRCh38.p12 chr8: 129,850,847-145,070,385 LOC105375784, CYP11B2, 253 more genes
    nsv6312709copy number variation2nstd102humanPathogenic GRCh37 chr8: 144,295,143-145,701,139 , GRCh38.p12 chr8: 143,213,268-144,475,756 MIR10400, BOP1, 83 more genes
    nsv6312626copy number variation3nstd102humanUncertain significance GRCh37 chr8: 143,822,561-145,743,168 , GRCh38.p12 chr8: 142,741,143-144,517,784 PYCR3, LOC101928902, 110 more genes
    nsv6270035copy number variation1nstd214human GRCh38 chr8: 143,981,404-143,981,591 , GRCh37.p13 chr8: 145,055,572-145,055,759 , GRCh37.p13 chr8|NW_003315923.1: 320,049-320,236 PARP10
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