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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
    nsv7067341inversion1nstd229human GRCh38 chr8: 90,646,482-90,649,843 , GRCh37.p13 chr8: 91,658,710-91,662,071 TMEM64
    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
    nsv7059000inversion1nstd229human GRCh38 chr8: 90,636,274-90,640,286 , GRCh37.p13 chr8: 91,648,502-91,652,514 TMEM64
    nsv6849165copy number variation1nstd229human GRCh38 chr8: 90,634,829-90,635,309 , GRCh37.p13 chr8: 91,647,057-91,647,537 TMEM64
    nsv6845272copy number variation1nstd229human GRCh38 chr8: 90,559,393-90,623,517 , GRCh37.p13 chr8: 91,571,621-91,635,745 LINC01030, TMEM64
    nsv6637803copy number variation1nstd102humanUncertain significance GRCh37 chr8: 87,010,235-91,879,538 , GRCh38.p12 chr8: 85,998,006-90,867,310 LOC105375633, NTAN1P2, 49 more genes
    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
    nsv6633365copy number variation1nstd224human GRCh37 chr8: 91,637,924-91,878,882 , GRCh38.p12 chr8: 90,625,696-90,866,654 LOC105375633, LOC105375634, 3 more genes
    nsv6633286copy number variation1nstd224human GRCh37 chr8: 91,637,924-91,817,642 , GRCh38.p12 chr8: 90,625,696-90,805,414 LOC105375633, NECAB1, 2 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
    nsv6435155copy number variation1nstd223human GRCh38 chr8: 90,643,601-90,645,500 , GRCh37.p13 chr8: 91,655,829-91,657,728 TMEM64
    nsv6424550copy number variation1nstd223human GRCh38 chr8: 90,620,012-90,620,369 , GRCh37.p13 chr8: 91,632,240-91,632,597 TMEM64
    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
    nsv6137316copy number variation1nstd213human GRCh37 chr8: 91,530,000-91,640,001 , GRCh38.p12 chr8: 90,517,772-90,627,773 TMEM64, LINC01030
    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
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