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Items: 1 to 20 of 182

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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
    nsv7070426inversion1nstd229human GRCh38 chr22: 30,413,817-30,419,957 , GRCh37.p13 chr22: 30,809,806-30,815,946 SEC14L2, RNU6-564P
    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
    nsv7036353copy number variation1nstd229human GRCh38 chr22: 30,418,019-30,429,006 , GRCh37.p13 chr22: 30,814,008-30,824,993 SEC14L2, MTFP1, 1 more genes
    nsv7020792copy number variation1nstd229human GRCh38 chr22: 30,335,406-30,530,242 , GRCh37.p13 chr22: 30,731,395-30,926,229 SEC14L3, SEC14L2, 13 more genes
    nsv7020536copy number variation1nstd229human GRCh38 chr22: 30,409,901-30,418,300 , GRCh37.p13 chr22: 30,805,890-30,814,289 SEC14L2
    nsv6638056copy number variation1nstd102humanUncertain significance GRCh37 chr22: 30,649,178-31,035,087 , GRCh38.p12 chr22: 30,253,189-30,639,100 GAL3ST1, SDC4P, 22 more genes
    nsv6544435copy number variation1nstd223human GRCh38 chr22: 30,409,881-30,418,306 , GRCh37.p13 chr22: 30,805,870-30,814,295 SEC14L2
    nsv6542890copy number variation1nstd223human GRCh38 chr22: 30,411,563-30,412,578 , GRCh37.p13 chr22: 30,807,552-30,808,567 SEC14L2
    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
    nsv6252068mobile element insertion1nstd215human GRCh38 chr22: 30,425,523-30,425,523 , GRCh37.p13 chr22: 30,821,511-30,821,511 MTFP1, SEC14L2
    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
    nsv6102633insertion1nstd212human GRCh38 chr22: 30,402,758-30,402,758 , GRCh37.p13 chr22: 30,798,747-30,798,747 SEC14L2
    nsv5375659translocation1nstd200human GRCh38 chr22: 30,420,165-30,420,165 , GRCh38 chr22: 30,419,956-30,419,956 , GRCh37.p13 chr22: 30,816,154-30,816,154 , GRCh37.p13 chr22: 30,815,945-30,815,945 , SEC14L2, 1 more genes
    nsv5375658translocation1nstd200human GRCh38 chr22: 30,413,611-30,413,611 , GRCh38 chr22: 30,414,352-30,414,352 , GRCh37.p13 chr22: 30,810,341-30,810,341 , GRCh37.p13 chr22: 30,809,600-30,809,600 SEC14L2
    nsv5039697copy number variation1nstd200human GRCh38 chr22: 30,418,010-30,429,009 , GRCh37.p13 chr22: 30,813,999-30,824,996 , RNU6-564P, 2 more genes
    nsv5036168copy number variation1nstd200human GRCh38 chr22: 30,378,114-30,449,390 , GRCh37.p13 chr22: 30,774,103-30,845,377 , SEC14L3, 9 more genes
    nsv5032148copy number variation1nstd200human GRCh38 chr22: 30,409,881-30,418,306 , GRCh37.p13 chr22: 30,805,870-30,814,295 SEC14L2
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