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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7077895inversion1nstd229human GRCh38 chr20: 265,739-1,834,868 , GRCh37.p13 chr20: 246,380-1,815,514 PSMF1, LOC105372498, 46 more genes
    nsv7059236inversion1nstd229human GRCh38 chr20: 589,971-675,712 , GRCh37.p13 chr20: 570,615-656,356 LOC107985423, TCF15, 2 more genes
    nsv7012737copy number variation1nstd229human GRCh38 chr20: 384,285-773,654 , GRCh37.p13 chr20: 364,929-754,298 SRXN1, RBCK1, 7 more genes
    nsv7007834copy number variation1nstd229human GRCh38 chr20: 208,997-952,202 , GRCh37.p13 chr20: 189,638-932,845 TBC1D20, NRSN2-AS1, 19 more genes
    nsv7001934copy number variation1nstd229human GRCh38 chr20: 517,901-745,400 , GRCh37.p13 chr20: 498,545-726,044 SCRT2, SRXN1, 3 more genes
    nsv7001400copy number variation1nstd229human GRCh38 chr20: 601,493-603,123 , GRCh37.p13 chr20: 582,137-583,767 TCF15
    nsv6637610copy number variation1nstd102humanUncertain significance GRCh37 chr20: 384,444-744,450 , GRCh38.p12 chr20: 403,800-763,806 SCRT2, TBC1D20, 6 more genes
    nsv6637401copy number variation1nstd102humanUncertain significance GRCh37 chr20: 404,407-611,731 , GRCh38.p12 chr20: 423,763-631,087 TBC1D20, RBCK1, 2 more genes
    nsv6521737copy number variation1nstd223human GRCh38 chr20: 596,427-614,460 , GRCh37.p13 chr20: 577,071-595,104 TCF15
    nsv6516354copy number variation1nstd223human GRCh38 chr20: 318,748-687,991 , GRCh37.p13 chr20: 299,392-668,635 NRSN2, TCF15, 10 more genes
    nsv6315567copy number variation1nstd102humanPathogenic GRCh38 chr20: 453,176-822,262 , GRCh37.p13 chr20: 433,820-802,905 CSNK2A1, TCF15, 5 more genes
    nsv6315181copy number variation1nstd102humanUncertain significance GRCh37 chr20: 489,033-898,472 , GRCh38.p12 chr20: 508,389-917,829 RPS10P5, CSNK2A1, 8 more genes
    nsv6314010copy number variation1nstd102humanUncertain significance GRCh37 chr20: 242,496-742,740 , GRCh38.p12 chr20: 261,855-762,096 C20orf96, RBCK1, 13 more genes
    nsv6311232copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chr20: 389,402-746,418 , GRCh38.p12 chr20: 408,758-765,774 CSNK2A1, TCF15, 6 more genes
    nsv6134293copy number variation1nstd213human GRCh37 chr20: 390,000-670,001 , GRCh38.p12 chr20: 409,356-689,357 CSNK2A1, TCF15, 5 more genes
    nsv6134291copy number variation1nstd213human GRCh37 chr20: 370,000-860,001 , GRCh38.p12 chr20: 389,356-879,358 CSNK2A1, TRIB3, 10 more genes
    nsv6134166copy number variation1nstd213human GRCh37 chr20: 480,000-620,001 , GRCh38.p12 chr20: 499,356-639,357 CSNK2A1, TCF15
    nsv6133904copy number variation1nstd213human GRCh37 chr20: 1-1,970,001 , GRCh38.p12 chr20: 79,361-1,989,355 , CSNK2A1, 57 more genes
    nsv5711941mobile element insertion2nstd211human GRCh38 chr20: 609,507-609,507 , GRCh37.p13 chr20: 590,151-590,151 TCF15
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