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Items: 1 to 20 of 199

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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
    nsv7069591inversion1nstd229human GRCh38 chr20: 105,288-375,237 , GRCh37.p13 chr20: 85,929-355,881 DEFB126, DEFB128, 9 more genes
    nsv7015752copy number variation1nstd229human GRCh38 chr20: 319,231-322,821 , GRCh37.p13 chr20: 299,875-303,465 NRSN2-AS1
    nsv7015109copy number variation1nstd229human GRCh38 chr20: 212,701-479,100 , GRCh37.p13 chr20: 193,342-459,744 C20orf96, RBCK1, 10 more genes
    nsv7010119copy number variation1nstd229human GRCh38 chr20: 314,821-318,100 , GRCh37.p13 chr20: 295,465-298,744 NRSN2-AS1
    nsv7007834copy number variation1nstd229human GRCh38 chr20: 208,997-952,202 , GRCh37.p13 chr20: 189,638-932,845 TBC1D20, NRSN2-AS1, 19 more genes
    nsv6999090copy number variation1nstd229human GRCh38 chr20: 318,813-319,186 , GRCh37.p13 chr20: 299,457-299,830 NRSN2-AS1
    nsv6637884copy number variation1nstd102humanUncertain significance GRCh37 chr20: 79,455-347,319 , GRCh38.p12 chr20: 98,814-366,675 DEFB126, ZCCHC3, 9 more genes
    nsv6528580copy number variation1nstd223human GRCh38 chr20: 317,165-319,598 , GRCh37.p13 chr20: 297,809-300,242 NRSN2-AS1
    nsv6527300copy number variation1nstd223human GRCh38 chr20: 320,177-321,123 , GRCh37.p13 chr20: 300,821-301,767 NRSN2-AS1
    nsv6526695copy number variation1nstd223human GRCh38 chr20: 319,135-319,534 , GRCh37.p13 chr20: 299,779-300,178 NRSN2-AS1
    nsv6525928copy number variation1nstd223human GRCh38 chr20: 319,405-320,977 , GRCh37.p13 chr20: 300,049-301,621 NRSN2-AS1
    nsv6516354copy number variation1nstd223human GRCh38 chr20: 318,748-687,991 , GRCh37.p13 chr20: 299,392-668,635 NRSN2, TCF15, 10 more genes
    nsv6314010copy number variation1nstd102humanUncertain significance GRCh37 chr20: 242,496-742,740 , GRCh38.p12 chr20: 261,855-762,096 C20orf96, RBCK1, 13 more genes
    nsv6134047copy number variation1nstd213human GRCh37 chr20: 60,000-470,001 , GRCh38.p12 chr20: 79,361-489,357 RBCK1, DEFB126, 14 more genes
    nsv6133904copy number variation1nstd213human GRCh37 chr20: 1-1,970,001 , GRCh38.p12 chr20: 79,361-1,989,355 , CSNK2A1, 57 more genes
    nsv5562784sequence alteration1nstd206human GRCh38 chr20: 325,118-325,725 , GRCh37.p13 chr20: 305,762-306,369 SOX12, NRSN2-AS1
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5531194copy number variation1nstd206human GRCh38 chr20: 319,166-320,180 , GRCh37.p13 chr20: 299,810-300,824 NRSN2-AS1
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