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Items: 1 to 20 of 266

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7074963inversion1nstd229human GRCh38 chr22: 31,201,802-31,493,198 , GRCh37.p13 chr22: 31,597,788-31,889,184 PPP1R14BP1, PIK3IP1, 12 more genes
    nsv7071415inversion1nstd229human GRCh38 chr22: 31,272,718-31,273,402 , GRCh37.p13 chr22: 31,668,704-31,669,388 LIMK2
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 more genes
    nsv7067688inversion1nstd229human GRCh38 chr22: 31,255,174-31,266,900 , GRCh37.p13 chr22: 31,651,160-31,662,886 LIMK2
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7060425inversion1nstd229human GRCh38 chr22: 31,260,924-31,266,719 , GRCh37.p13 chr22: 31,656,910-31,662,705 LIMK2
    nsv7037154copy number variation1nstd229human GRCh38 chr22: 31,269,921-31,269,978 , GRCh37.p13 chr22: 31,665,907-31,665,964 LIMK2
    nsv7026923copy number variation1nstd229human GRCh38 chr22: 31,213,001-31,227,700 , GRCh37.p13 chr22: 31,608,987-31,623,686 RNU6-1128P, LIMK2
    nsv7024391copy number variation1nstd229human GRCh38 chr22: 31,232,631-31,237,208 , GRCh37.p13 chr22: 31,628,617-31,633,194 LIMK2
    nsv7021538copy number variation1nstd229human GRCh38 chr22: 31,218,287-31,227,375 , GRCh37.p13 chr22: 31,614,273-31,623,361 RNU6-1128P, LIMK2
    nsv6598251inversion1nstd223human GRCh38 chr22: 31,234,017-31,234,681 , GRCh37.p13 chr22: 31,630,003-31,630,667 LIMK2
    nsv6546578copy number variation1nstd223human GRCh38 chr22: 31,273,947-31,274,650 , GRCh37.p13 chr22: 31,669,933-31,670,636 PPP1R14BP1, LIMK2
    nsv6314421complex chromosomal rearrangement3nstd102humanUncertain significance GRCh38.p12 chr22: 31,226,472-31,226,472 , GRCh38.p12 chr22: 31,226,484-31,226,484 , GRCh38.p12 chr22: 31,226,484-31,226,484 , GRCh38.p12 chr22: 31,226,615-31,226,615 , GRCh37 chr22: 31,622,458-31,622,458 , GRCh37 chr22: 31,622,470-31,622,470 , GRCh37 chr22: 31,622,470-31,622,470 , GRCh37 chr22: 31,622,601-31,622,601 , GRCh37 chrX: 62,683,198-62,683,198 , GRCh37 chrX: 62,683,200-62,683,200 , GRCh38.p12 chrX: 63,463,318-63,463,318 , GRCh38.p12 chrX: 63,463,320-63,463,320 LIMK2, LINC01278
    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
    nsv6222113copy number variation1nstd214human GRCh38 chr22: 31,269,916-31,269,977 , GRCh37.p13 chr22: 31,665,902-31,665,963 LIMK2
    nsv6146929copy number variation1nstd206human GRCh38 chr22: 31,269,921-31,269,978 , GRCh37.p13 chr22: 31,665,907-31,665,964 LIMK2
    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
    nsv6131281insertion1nstd186human GRCh37 chr22: 31,622,461-31,622,461 , GRCh38.p12 chr22: 31,226,475-31,226,475 LIMK2
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