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Items: 1 to 20 of 416

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7139847insertion1nstd232human GRCh37.p13 chr8: 21,551,294-21,551,294 , GRCh38.p12 chr8: 21,693,782-21,693,782 GFRA2
    nsv7072905inversion1nstd229human GRCh38 chr8: 21,785,200-21,791,704 , GRCh37.p13 chr8: 21,642,712-21,649,216 GFRA2
    nsv7069944inversion1nstd229human GRCh38 chr8: 21,780,162-21,785,301 , GRCh37.p13 chr8: 21,637,674-21,642,813 GFRA2
    nsv6857968copy number variation1nstd229human GRCh38 chr8: 21,604,801-21,920,400 , GRCh37.p13 chr8: 21,462,312-21,777,911 OR6R2P, DOK2, 3 more genes
    nsv6856308copy number variation1nstd229human GRCh38 chr8: 21,682,921-21,707,858 , GRCh37.p13 chr8: 21,540,433-21,565,370 GFRA2
    nsv6856297copy number variation1nstd229human GRCh38 chr8: 21,697,213-21,698,001 , GRCh37.p13 chr8: 21,554,725-21,555,513 GFRA2
    nsv6853170copy number variation1nstd229human GRCh38 chr8: 21,740,404-21,777,598 , GRCh37.p13 chr8: 21,597,916-21,635,110 GFRA2
    nsv6852267copy number variation1nstd229human GRCh38 chr8: 21,303,011-21,729,672 , GRCh37.p13 chr8: 21,160,522-21,587,184 LINC03093, LOC107986922, 1 more genes
    nsv6851629copy number variation1nstd229human GRCh38 chr8: 21,719,031-21,720,905 , GRCh37.p13 chr8: 21,576,543-21,578,417 GFRA2
    nsv6850086copy number variation1nstd229human GRCh38 chr8: 21,722,480-21,726,901 , GRCh37.p13 chr8: 21,579,992-21,584,413 GFRA2
    nsv6846784copy number variation1nstd229human GRCh38 chr8: 21,761,701-21,786,200 , GRCh37.p13 chr8: 21,619,213-21,643,712 GFRA2
    nsv6843427copy number variation1nstd229human GRCh38 chr8: 21,749,780-21,792,372 , GRCh37.p13 chr8: 21,607,292-21,649,884 GFRA2
    nsv6842345copy number variation1nstd229human GRCh38 chr8: 21,739,201-22,308,765 , GRCh37.p13 chr8: 21,596,713-22,166,278 FHIP2B, FGF17, 17 more genes
    nsv6636877copy number variation1nstd102humanUncertain significance GRCh37 chr8: 21,448,263-21,710,793 , GRCh38.p12 chr8: 21,590,752-21,853,282 GFRA2, LOC107986922, 1 more genes
    nsv6636714copy number variation1nstd102humanUncertain significance GRCh37 chr8: 20,871,759-21,613,186 , GRCh38.p12 chr8: 21,014,248-21,755,674 LOC107986922, LINC03093, 1 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6632536copy number variation1nstd224human GRCh37 chr8: 21,352,198-21,640,407 , GRCh38.p12 chr8: 21,494,687-21,782,895 , GRCh38.p12 chr8|NW_017852932.1: 99,178-265,876 GFRA2, LOC107986922
    nsv6435134copy number variation1nstd223human GRCh38 chr8: 21,697,798-21,732,311 , GRCh37.p13 chr8: 21,555,310-21,589,823 GFRA2
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