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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3895167copy number variation1nstd102humanBenign GRCh37 chr20: 60,891,045-60,900,490 , GRCh38.p12 chr20: 62,315,989-62,325,434 LAMA5
    nsv3901767copy number variation1nstd102humanBenign GRCh37 chr20: 60,892,746-60,901,762 , GRCh38.p12 chr20: 62,317,690-62,326,706 LAMA5
    nsv3897012copy number variation1nstd102humanBenign GRCh37 chr20: 60,891,783-60,900,578 , GRCh38.p12 chr20: 62,316,727-62,325,522 LAMA5
    nsv3899024copy number variation1nstd102humanBenign GRCh37 chr20: 60,891,783-60,900,490 , GRCh38.p12 chr20: 62,316,727-62,325,434 LAMA5
    nsv3903334copy number variation1nstd102humanBenign GRCh37 chr20: 60,892,077-60,900,579 , GRCh38.p12 chr20: 62,317,021-62,325,523 LAMA5
    nsv3909771copy number variation1nstd102humanBenign GRCh37 chr20: 60,891,045-60,899,525 , GRCh38.p12 chr20: 62,315,989-62,324,469 LAMA5
    nsv3894400copy number variation1nstd102humanBenign GRCh37 chr20: 60,891,045-60,899,513 , GRCh38.p12 chr20: 62,315,989-62,324,457 LAMA5
    nsv3893948copy number variation1nstd102humanBenign GRCh37 chr20: 60,891,045-60,899,206 , GRCh38.p12 chr20: 62,315,989-62,324,150 LAMA5
    nsv3893551copy number variation1nstd102humanBenign GRCh37 chr20: 60,891,783-60,899,513 , GRCh38.p12 chr20: 62,316,727-62,324,457 LAMA5
    nsv3907476copy number variation1nstd102humanBenign GRCh37 chr20: 60,872,280-60,908,969 , GRCh38.p12 chr20: 62,297,224-62,333,913 LAMA5, MIR4758, 1 more genes
    nsv7096265copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,854,193-60,886,170 , GRCh38.p12 chr20: 62,279,137-62,311,114 LAMA5, OSBPL2, 1 more genes
    nsv7095800copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,861,619-60,890,283 , GRCh38.p12 chr20: 62,286,563-62,315,227 LAMA5, ADRM1, 1 more genes
    nsv3892750copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941 LAMA5, TGIF2-RAB5IF, 1314 more genes
    nsv3905072copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435 LAMA5, LRRN4, 1313 more genes
    nsv3895314copy number variation2nstd102humanPathogenic GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202 LAMA5, PKIG, 1311 more genes
    nsv3896520copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110 LAMA5, COMMD7, 1311 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 LAMA5, MIR3646, 1310 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 LAMA5, FTLP1, 472 more genes
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LAMA5, LINC01742, 253 more genes
    nsv3911673copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,773,088-62,908,674 , NCBI36 chr20: 54,206,495-62,379,118 , GRCh38 chr20: 56,198,032-64,277,321 LAMA5, LOC105372709, 226 more genes
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