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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137123copy number variation1nstd102humanPathogenic GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046 SLC26A7, LOC105375639, 112 more genes
    nsv7078060inversion1nstd229human GRCh38 chr8: 88,934,395-91,030,131 , GRCh37.p13 chr8: 89,946,624-92,042,359 RNA5SP273, LOC105375631, 21 more genes
    nsv7077999inversion1nstd229human GRCh38 chr8: 90,977,597-95,722,625 , GRCh37.p13 chr8: 91,989,825-96,734,853 LINC02894, MIR3150B, 70 more genes
    nsv7076164inversion1nstd229human GRCh38 chr8: 90,765,384-91,734,139 , GRCh37.p13 chr8: 91,777,612-92,746,367 LOC105375635, CPP, 12 more genes
    nsv7074278inversion1nstd229human GRCh38 chr8: 91,030,306-91,033,836 , GRCh37.p13 chr8: 92,042,534-92,046,064 PIP4P2
    nsv7063775inversion1nstd229human GRCh38 chr8: 90,028,515-91,181,513 , GRCh37.p13 chr8: 91,040,743-92,193,741 LOC107986955, OTUD6B-AS1, 15 more genes
    nsv7062896inversion1nstd229human GRCh38 chr8: 90,646,249-91,578,240 , GRCh37.p13 chr8: 91,658,477-92,590,468 C8orf88, TMEM64, 12 more genes
    nsv7058205inversion1nstd229human GRCh38 chr8: 90,920,330-91,789,769 , GRCh37.p13 chr8: 91,932,558-92,801,997 RN7SKP231, LOC105375634, 10 more genes
    nsv6845451copy number variation1nstd229human GRCh38 chr8: 91,036,148-91,036,479 , GRCh37.p13 chr8: 92,048,376-92,048,707 PIP4P2
    nsv6844270copy number variation1nstd229human GRCh38 chr8: 91,029,119-91,045,609 , GRCh37.p13 chr8: 92,041,347-92,057,837 PIP4P2
    nsv6843408copy number variation1nstd229human GRCh38 chr8: 91,018,601-91,022,400 , GRCh37.p13 chr8: 92,030,829-92,034,628 PIP4P2
    nsv6840422copy number variation1nstd229human GRCh38 chr8: 90,989,099-90,991,963 , GRCh37.p13 chr8: 92,001,327-92,004,191 PIP4P2
    nsv6838123copy number variation1nstd229human GRCh38 chr8: 91,027,427-91,027,678 , GRCh37.p13 chr8: 92,039,655-92,039,906 PIP4P2
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 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
    nsv6555776inversion1nstd223human GRCh38 chr8: 90,046,984-91,196,055 , GRCh37.p13 chr8: 91,059,212-92,208,283 CPP, TMEM64, 15 more genes
    nsv6435395copy number variation1nstd223human GRCh38 chr8: 91,029,116-91,045,611 , GRCh37.p13 chr8: 92,041,344-92,057,839 PIP4P2
    nsv6422322copy number variation1nstd223human GRCh38 chr8: 90,994,201-90,995,500 , GRCh37.p13 chr8: 92,006,429-92,007,728 PIP4P2
    nsv6422283copy number variation1nstd223human GRCh38 chr8: 90,994,758-90,995,364 , GRCh37.p13 chr8: 92,006,986-92,007,592 PIP4P2
    nsv6419178copy number variation1nstd223human GRCh38 chr8: 91,007,592-91,007,997 , GRCh37.p13 chr8: 92,019,820-92,020,225 PIP4P2
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