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Items: 1 to 20 of 181

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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
    nsv7065072inversion1nstd229human GRCh38 chr8: 90,662,757-90,982,091 , GRCh37.p13 chr8: 91,674,985-91,994,319 NECAB1, LOC105375635, 3 more genes
    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
    nsv6846916copy number variation1nstd229human GRCh38 chr8: 90,984,362-90,984,815 , GRCh37.p13 chr8: 91,996,590-91,997,043 C8orf88
    nsv6844480copy number variation1nstd229human GRCh38 chr8: 90,976,034-90,980,499 , GRCh37.p13 chr8: 91,988,262-91,992,727 C8orf88
    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
    nsv6427699copy number variation1nstd223human GRCh38 chr8: 90,975,604-90,976,247 , GRCh37.p13 chr8: 91,987,832-91,988,475 C8orf88
    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
    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
    nsv6136704copy number variation1nstd213human GRCh37 chr8: 91,640,000-92,390,001 , GRCh38.p12 chr8: 90,627,772-91,377,773 PIP4P2, CPP, 12 more genes
    nsv6136610copy number variation1nstd213human GRCh37 chr8: 89,510,000-92,250,001 , GRCh38.p12 chr8: 88,497,771-91,237,773 LRRC69, COX6B1P6, 29 more genes
    nsv6136607copy number variation1nstd213human GRCh37 chr8: 87,430,000-94,700,001 , GRCh38.p12 chr8: 86,417,771-93,687,773 CALB1, WWP1, 73 more genes
    nsv6136605copy number variation1nstd213human GRCh37 chr8: 86,730,000-120,700,001 , GRCh38.p12 chr8: 85,717,771-119,687,761 CALB1, CDH17, 421 more genes
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