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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949561insertion1nstd209human GRCh38 chr8: 30,064,552-30,064,552 , GRCh37.p13 chr8: 29,922,068-29,922,068 SARAF
    nsv5926823copy number variation1nstd209human GRCh38 chr8: 30,066,139-30,066,775 , GRCh37.p13 chr8: 29,923,655-29,924,291 SARAF
    nsv5921319copy number variation1nstd209human GRCh38 chr8: 30,063,912-30,065,985 , GRCh37.p13 chr8: 29,921,428-29,923,501 SARAF
    nsv5920464copy number variation1nstd209human GRCh38 chr8: 30,077,121-30,080,625 , GRCh37.p13 chr8: 29,934,637-29,938,141 SARAF
    nsv5909976copy number variation1nstd209human GRCh38 chr8: 30,066,917-30,069,639 , GRCh37.p13 chr8: 29,924,433-29,927,155 SARAF
    nsv5909746copy number variation1nstd209human GRCh38 chr8: 30,070,059-30,082,845 , GRCh37.p13 chr8: 29,927,575-29,940,361 SARAF
    nsv5854550copy number variation1nstd209human GRCh38 chr8: 30,077,097-30,080,646 , GRCh37.p13 chr8: 29,934,613-29,938,162 SARAF
    nsv5728375mobile element insertion1nstd211human GRCh38 chr8: 30,077,992-30,077,992 , GRCh37.p13 chr8: 29,935,508-29,935,508 SARAF
    nsv5482437copy number variation1nstd206human GRCh38 chr8: 30,063,915-30,065,986 , GRCh37.p13 chr8: 29,921,431-29,923,502 SARAF
    nsv5476096copy number variation1nstd206human GRCh38 chr8: 30,065,996-30,066,776 , GRCh37.p13 chr8: 29,923,512-29,924,292 SARAF
    nsv5379216translocation1nstd200human GRCh38 chr8: 30,070,060-30,070,060 , GRCh38 chr8: 30,082,846-30,082,846 , GRCh37.p13 chr8: 29,927,576-29,927,576 , GRCh37.p13 chr8: 29,940,362-29,940,362 SARAF
    nsv5379215translocation1nstd200human GRCh38 chr8: 30,066,920-30,066,920 , GRCh38 chr8: 30,069,640-30,069,640 , GRCh37.p13 chr8: 29,927,156-29,927,156 , GRCh37.p13 chr8: 29,924,436-29,924,436 SARAF
    nsv5379214translocation1nstd200human GRCh38 chr8: 30,065,986-30,065,986 , GRCh38 chr8: 30,063,915-30,063,915 , GRCh37.p13 chr8: 29,923,502-29,923,502 , GRCh37.p13 chr8: 29,921,431-29,921,431 SARAF
    nsv5336586translocation1nstd200human GRCh37 chr8: 29,927,156-29,927,156 , GRCh37 chr8: 29,924,436-29,924,436 , GRCh38.p12 chr8: 30,069,640-30,069,640 , GRCh38.p12 chr8: 30,066,920-30,066,920 SARAF
    nsv5335932translocation1nstd200human GRCh37 chr8: 29,921,431-29,921,431 , GRCh37 chr8: 29,923,502-29,923,502 , GRCh38.p12 chr8: 30,063,915-30,063,915 , GRCh38.p12 chr8: 30,065,986-30,065,986 SARAF
    nsv5334119translocation1nstd200human GRCh37 chr8: 29,940,362-29,940,362 , GRCh37 chr8: 29,927,576-29,927,576 , GRCh38.p12 chr8: 30,070,060-30,070,060 , GRCh38.p12 chr8: 30,082,846-30,082,846 SARAF
    nsv5329430translocation1nstd204human GRCh38.p13 chr8: 30,070,060-30,070,060 , GRCh38.p13 chr8: 30,082,846-30,082,846 , GRCh37.p13 chr8: 29,927,576-29,927,576 , GRCh37.p13 chr8: 29,940,362-29,940,362 SARAF
    nsv5322117translocation1nstd204human GRCh38.p13 chr8: 30,066,920-30,066,920 , GRCh38.p13 chr8: 30,069,640-30,069,640 , GRCh37.p13 chr8: 29,927,156-29,927,156 , GRCh37.p13 chr8: 29,924,436-29,924,436 SARAF
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5106284mobile element insertion1nstd203human GRCh38 chr8: 30,064,561-30,064,579 , GRCh37.p13 chr8: 29,922,077-29,922,095 SARAF
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