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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095832copy number variation1nstd102humanUncertain significance GRCh37 chr22: 32,500,753-32,894,517 , GRCh38.p12 chr22: 32,104,766-32,498,530 IGLCOR22-2, AP1B1P2, 16 more genes
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7070215inversion1nstd229human GRCh38 chr22: 32,498,838-32,517,580 , GRCh37.p13 chr22: 32,894,825-32,913,567 FBXO7, SYN3
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7064427inversion1nstd229human GRCh38 chr22: 32,257,546-32,480,102 , GRCh37.p13 chr22: 32,653,533-32,876,089 RFPL3S, BPIFC, 10 more genes
    nsv7031024copy number variation1nstd229human GRCh38 chr22: 32,471,137-32,480,317 , GRCh37.p13 chr22: 32,867,124-32,876,304 FBXO7
    nsv7024831copy number variation1nstd229human GRCh38 chr22: 32,494,190-32,494,658 , GRCh37.p13 chr22: 32,890,177-32,890,645 FBXO7
    nsv6544657copy number variation1nstd223human GRCh38 chr22: 32,472,401-32,478,000 , GRCh37.p13 chr22: 32,868,388-32,873,987 FBXO7
    nsv6311321copy number variation1nstd102humanUncertain significance GRCh37 chr22: 32,232,938-34,157,463 , GRCh38.p12 chr22: 31,836,952-33,761,476 SYN3, DEPDC5, 36 more genes
    nsv6311268copy number variation1nstd102humanUncertain significance GRCh37 chr22: 32,870,990-32,875,282 , GRCh38.p12 chr22: 32,475,003-32,479,295 FBXO7
    nsv6311263copy number variation1nstd102humanUncertain significance GRCh37 chr22: 29,083,885-34,046,674 , GRCh38.p12 chr22: 28,687,897-33,650,688 SNORD125, LOC107985533, 145 more genes
    nsv6252089mobile element insertion1nstd215human GRCh38 chr22: 32,482,493-32,482,493 , GRCh37.p13 chr22: 32,878,480-32,878,480 FBXO7
    nsv6252088mobile element insertion1nstd215human GRCh38 chr22: 32,475,820-32,475,820 , GRCh37.p13 chr22: 32,871,807-32,871,807 FBXO7
    nsv6212664copy number variation1nstd214human GRCh38 chr22: 32,491,562-32,491,619 , GRCh37.p13 chr22: 32,887,549-32,887,606 FBXO7
    nsv6134210copy number variation1nstd213human GRCh37 chr22: 30,130,000-36,350,001 , GRCh38.p12 chr22: 29,734,011-35,953,953 HMOX1, LIF, 146 more genes
    nsv6134118copy number variation1nstd213human GRCh37 chr22: 27,870,000-35,640,001 , GRCh38.p12 chr22: 27,474,039-35,244,008 AP1B1, EWSR1, 172 more genes
    nsv6103892insertion1nstd212human GRCh38 chr22: 32,491,586-32,491,586 , GRCh37.p13 chr22: 32,887,573-32,887,573 FBXO7
    nsv6046193copy number variation1nstd212human GRCh38 chr22: 32,410,864-32,473,570 , GRCh37.p13 chr22: 32,806,851-32,869,557 FBXO7, RTCB, 1 more genes
    nsv5722278mobile element insertion1nstd211human GRCh38 chr22: 32,484,716-32,484,716 , GRCh37.p13 chr22: 32,880,703-32,880,703 FBXO7
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