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Items: 1 to 20 of 295

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7075635inversion1nstd229human GRCh38 chr8: 143,728,678-143,739,693 , GRCh37.p13 chr8: 144,810,848-144,821,863 , GRCh37.p13 chr8|NW_003315923.1: 67,323-78,338 MIR4664, FAM83H
    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
    nsv6866783copy number variation1nstd229human GRCh38 chr8: 143,699,101-143,748,400 , GRCh37.p13 chr8|NW_003315923.1: 37,746-87,045 , GRCh37.p13 chr8: 144,781,271-144,830,570 CCDC166, MAPK15, 3 more genes
    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
    nsv6632682copy number variation1nstd224human GRCh37 chr8: 144,812,307-144,893,317 , GRCh38.p12 chr8: 143,730,137-143,811,147 , GRCh38.p12 chr8|NT_187571.1: 207,184-288,194 SCRIB, FAM83H, 4 more genes
    nsv6632505copy number variation1nstd224human GRCh37 chr8: 144,808,779-144,893,084 , GRCh38.p12 chr8: 143,726,609-143,810,914 , GRCh38.p12 chr8|NT_187571.1: 203,656-287,961 FAM83H, SCRIB, 3 more genes
    nsv6632504copy number variation1nstd224human GRCh37 chr8: 144,547,942-144,811,340 , GRCh38.p12 chr8: 143,465,772-143,729,170 , GRCh38.p12 chr8|NT_187571.1: 1-206,217 GFUS, ZC3H3, 18 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
    nsv6435049copy number variation1nstd223human GRCh38 chr8: 143,430,801-143,727,600 , GRCh37.p13 chr8: 144,512,971-144,743,525 MAFA, MROH6, 19 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
    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
    nsv6136343copy number variation1nstd213human GRCh37 chr8: 144,780,000-144,920,001 , GRCh38.p12 chr8: 143,697,830-143,837,829 , GRCh38.p12 chr8|NT_187571.1: 174,877-305,841 SCRIB, IQANK1, 12 more genes
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