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Items: 1 to 20 of 907

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130861mobile element insertion1nstd186human GRCh37 chr22: 19,210,913-19,210,964 , GRCh38.p12 chr22: 19,223,390-19,223,441 CLTCL1
    nsv6130794insertion1nstd186human GRCh37 chr22: 19,178,131-19,178,162 , GRCh38.p12 chr22: 19,190,619-19,190,652 CLTCL1
    nsv6126277copy number variation1nstd186human GRCh37 chr22: 19,247,916-19,248,102 , GRCh38.p12 chr22: 19,260,393-19,260,579 CLTCL1
    nsv6113076mobile element insertion1nstd186human GRCh37 chr22: 19,238,703-19,238,703 , GRCh38.p12 chr22: 19,251,180-19,251,180 DVL1P1, CLTCL1
    nsv6112800copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,977-21,463,189 , GRCh38.p12 chr22: 18,339,130-21,108,900 MIR4761, TUBA3FP, 124 more genes
    nsv6112793copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,693-21,465,485 , GRCh38.p12 chr22: 18,339,130-21,111,196 THAP7, LOC100129262, 125 more genes
    nsv6112781copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,841,374-21,465,101 , GRCh38.p12 chr22: 18,339,130-21,110,812 SEPTIN5, RNU6-225P, 125 more genes
    nsv6112779copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,571-21,464,697 , GRCh38.p12 chr22: 18,339,130-21,110,408 PRODH, MIR3618, 124 more genes
    nsv5980452copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,969-21,462,658 , GRCh38.p12 chr22: 18,339,130-21,108,369 LINC01637, BCRP7, 124 more genes
    nsv5976399inversion1nstd209human GRCh38 chr22: 17,577,704-20,098,016 , GRCh37.p13 chr22: 18,057,770-20,703,815 , ARVCF, 90 more genes
    nsv5971819insertion1nstd209human GRCh38 chr22: 19,251,180-19,251,180 , GRCh37.p13 chr22|NW_003871096.1: 104,397-104,397 , GRCh37.p13 chr22: 19,238,703-19,238,703 CLTCL1, DVL1P1
    nsv5969586insertion1nstd209human GRCh38 chr22: 19,223,372-19,223,372 , GRCh37.p13 chr22: 19,210,895-19,210,895 , GRCh37.p13 chr22|NW_003871096.1: 76,589-76,589 CLTCL1
    nsv5960679copy number variation1nstd209human GRCh38 chr22: 19,257,319-19,263,421 , GRCh37.p13 chr22: 19,244,842-19,250,944 , GRCh37.p13 chr22|NW_003871096.1: 110,536-116,638 CLTCL1, KRT18P62
    nsv5955599copy number variation1nstd209human GRCh38 chr22: 19,212,558-19,212,614 , GRCh37.p13 chr22: 19,200,067-19,200,123 , GRCh37.p13 chr22|NW_003871096.1: 65,775-65,831 CLTCL1
    nsv5954425copy number variation1nstd209human GRCh38 chr22: 19,188,156-19,188,241 , GRCh37.p13 chr22|NW_003871096.1: 41,373-41,458 , GRCh37.p13 chr22: 19,175,668-19,175,753 CLTCL1
    nsv5953682copy number variation1nstd209human GRCh38 chr22: 19,185,350-19,186,623 , GRCh37.p13 chr22|NW_003871096.1: 38,567-39,840 , GRCh37.p13 chr22: 19,172,862-19,174,135 CLTCL1
    nsv5950632copy number variation1nstd209human GRCh38 chr22: 19,260,392-19,260,578 , GRCh37.p13 chr22: 19,247,915-19,248,101 , GRCh37.p13 chr22|NW_003871096.1: 113,609-113,795 CLTCL1
    nsv5947825copy number variation1nstd209human GRCh38 chr22: 19,270,566-19,297,892 , GRCh37.p13 chr22: 19,258,089-19,285,415 , GRCh37.p13 chr22|NW_003871096.1: 123,783-151,109 LOC105372859, CLTCL1
    nsv5887154copy number variation2nstd209human GRCh38 chr22: 19,288,610-19,290,509 , GRCh37.p13 chr22: 19,276,133-19,278,032 , GRCh37.p13 chr22|NW_003871096.1: 141,827-143,726 LOC105372859, CLTCL1
    nsv5885787copy number variation1nstd209human GRCh38 chr22: 19,291,732-19,293,004 , GRCh37.p13 chr22|NW_003871096.1: 144,949-146,221 , GRCh37.p13 chr22: 19,279,255-19,280,527 LOC105372859, CLTCL1
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