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Items: 1 to 20 of 662

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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
    nsv7148110copy number variation1nstd102humanPathogenic GRCh37 chr8: 7,080,281-12,045,269 , GRCh38.p12 chr8: 7,222,759-12,187,760 DEFB106A, LOC101927997, 176 more genes
    nsv7077850inversion1nstd229human GRCh38 chr8: 11,437,533-11,440,997 , GRCh37.p13 chr8: 11,295,042-11,298,506 FAM167A, FAM167A-AS1
    nsv7071134inversion1nstd229human GRCh38 chr8: 11,401,622-11,401,657 , GRCh37.p13 chr8: 11,259,131-11,259,166 FAM167A-AS1
    nsv7070191inversion1nstd229human GRCh38 chr8: 11,431,142-11,714,759 , GRCh37.p13 chr8: 11,288,651-11,572,268 BLK, GATA4, 6 more genes
    nsv7069609inversion1nstd229human GRCh38 chr8: 7,102,414-12,683,056 , GRCh37.p13 chr8: 6,959,936-12,540,565 FAM90A20, LOC107986910, 201 more genes
    nsv7067997inversion1nstd229human GRCh38 chr8: 8,181,479-12,388,066 , GRCh37.p13 chr8: 8,039,001-12,245,575 TNKS, ZNF705D, 113 more genes
    nsv7066304inversion1nstd229human GRCh38 chr8: 11,425,112-11,425,148 , GRCh37.p13 chr8: 11,282,621-11,282,657 FAM167A, FAM167A-AS1
    nsv7065354inversion1nstd229human GRCh38 chr8: 9,129,798-15,405,439 , GRCh37.p13 chr8: 8,987,308-15,262,948 FAM167A, LOC729732, 132 more genes
    nsv7062538inversion1nstd229human GRCh38 chr8: 7,137,678-12,551,118 , GRCh37.p13 chr8: 6,995,200-12,408,627 MIR124-1, MFHAS1, 197 more genes
    nsv7060774inversion1nstd229human GRCh38 chr8: 7,366,932-11,853,836 , GRCh37.p13 chr8: 7,224,454-11,711,345 DEFB104B, SNORA99, 135 more genes
    nsv7059146inversion1nstd229human GRCh38 chr8: 7,352,588-12,547,775 , GRCh37.p13 chr8: 7,210,110-12,405,284 LOC107986910, HSPD1P2, 179 more genes
    nsv7058956inversion1nstd229human GRCh38 chr8: 8,224,000-12,734,745 , GRCh37.p13 chr8: 8,081,522-12,592,254 MIR3926-1, FAM90A25P, 129 more genes
    nsv6857518copy number variation1nstd229human GRCh38 chr8: 11,370,853-11,371,767 , GRCh37.p13 chr8: 11,228,362-11,229,276 FAM167A-AS1
    nsv6856826copy number variation1nstd229human GRCh38 chr8: 11,331,493-11,439,724 , GRCh37.p13 chr8: 11,189,002-11,297,233 RN7SL293P, FAM167A, 5 more genes
    nsv6856309copy number variation1nstd229human GRCh38 chr8: 11,426,577-11,426,607 , GRCh37.p13 chr8: 11,284,086-11,284,116 FAM167A, FAM167A-AS1
    nsv6856029copy number variation1nstd229human GRCh38 chr8: 11,400,454-11,425,160 , GRCh37.p13 chr8: 11,257,963-11,282,669 FAM167A, FAM167A-AS1
    nsv6855586copy number variation1nstd229human GRCh38 chr8: 11,379,843-11,379,919 , GRCh37.p13 chr8: 11,237,352-11,237,428 FAM167A-AS1, RN7SL293P
    nsv6854842copy number variation1nstd229human GRCh38 chr8: 11,371,501-11,377,700 , GRCh37.p13 chr8: 11,229,010-11,235,209 RN7SL293P, FAM167A-AS1
    nsv6854553copy number variation1nstd229human GRCh38 chr8: 11,429,663-11,432,310 , GRCh37.p13 chr8: 11,287,172-11,289,819 FAM167A, FAM167A-AS1
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