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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148124copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500 LINC02964, TATDN1, 115 more genes
    nsv7064603inversion1nstd229human GRCh38 chr8: 121,321,668-121,392,361 , GRCh37.p13 chr8: 122,333,908-122,404,601 RPL35AP19
    nsv7064459inversion1nstd229human GRCh38 chr8: 121,307,206-121,387,713 , GRCh37.p13 chr8: 122,319,446-122,399,953 RPL35AP19
    nsv6854920copy number variation1nstd229human GRCh38 chr8: 120,966,661-121,475,655 , GRCh37.p13 chr8: 121,978,901-122,487,895 LOC105375731, LOC100133147, 1 more genes
    nsv6844446copy number variation1nstd229human GRCh38 chr8: 121,351,561-121,378,390 , GRCh37.p13 chr8: 122,363,801-122,390,630 RPL35AP19
    nsv6840685copy number variation1nstd229human GRCh38 chr8: 120,965,101-121,400,300 , GRCh37.p13 chr8: 121,977,341-122,412,540 RPL35AP19, LOC105375731, 1 more genes
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 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
    nsv6632659copy number variation1nstd224human GRCh37 chr8: 122,339,597-122,398,763 , GRCh38.p12 chr8: 121,327,357-121,386,523 RPL35AP19
    nsv6632658copy number variation1nstd224human GRCh37 chr8: 122,322,450-122,394,987 , GRCh38.p12 chr8: 121,310,210-121,382,747 RPL35AP19
    nsv6571163inversion1nstd223human GRCh38 chr8: 121,321,661-121,392,361 , GRCh37.p13 chr8: 122,333,901-122,404,601 RPL35AP19
    nsv6420330copy number variation1nstd223human GRCh38 chr8: 121,343,939-121,545,885 , GRCh37.p13 chr8: 122,356,179-122,558,125 RPL35AP19
    nsv6417734copy number variation1nstd223human GRCh38 chr8: 121,351,561-121,378,387 , GRCh37.p13 chr8: 122,363,801-122,390,627 RPL35AP19
    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
    nsv6137041copy number variation1nstd213human GRCh37 chr8: 122,320,000-123,760,001 , GRCh38.p12 chr8: 121,307,760-122,747,762 LOC105375733, MRPS36P3, 8 more genes
    nsv6136307copy number variation1nstd213human GRCh37 chr8: 122,000,000-122,490,001 , GRCh38.p12 chr8: 120,987,760-121,477,761 LOC100133147, RPL35AP19, 1 more genes
    nsv6136306copy number variation1nstd213human GRCh37 chr8: 121,950,000-122,860,001 , GRCh38.p12 chr8: 120,937,760-121,847,762 HAS2, HAS2-AS1, 4 more genes
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