U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 649

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137204copy number variation1nstd102humanPathogenic GRCh37 chr11: 268,586-748,873 , GRCh38.p12 chr11: 268,586-748,873 PKP3, RN7SL838P, 32 more genes
    nsv7137059copy number variation1nstd102humanLikely benign GRCh37 chr11: 530,419-530,474 , GRCh38 chr11: 530,419-530,474 HRAS, LRRC56
    nsv7094089copy number variation2nstd102humanUncertain significance GRCh37 chr11: 532,636-554,276 , GRCh38.p12 chr11: 532,636-554,276 , GRCh38.p12 chr11|NT_187586.1: 62,277-83,916 LRRC56, LMNTD2, 1 more genes
    nsv7093693copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,636-819,925 , GRCh38.p12 chr11: 532,636-819,925 , GRCh38.p12 chr11|NT_187586.1: 62,277-209,248 HRAS, LRRC56, 25 more genes
    nsv7093222copy number variation1nstd102humanUncertain significance GRCh38 chr11: 533,463-533,464 , GRCh37 chr11: 533,463-533,464 HRAS, LRRC56
    nsv7073154inversion1nstd229human GRCh38 chr11: 516,385-567,173 , GRCh37.p13 chr11: 516,385-567,173 LRRC56, LMNTD2, 5 more genes
    nsv7068392inversion1nstd229human GRCh38 chr11: 260,223-620,051 , GRCh37.p13 chr11: 260,223-620,051 MIR210, LMNTD2-AS1, 25 more genes
    nsv7068164inversion1nstd229human GRCh38 chr11: 525,138-982,890 , GRCh37.p13 chr11: 525,138-982,890 DRD4, LMNTD2-AS1, 32 more genes
    nsv7067944inversion1nstd229human GRCh38 chr11: 288,558-695,861 , GRCh37.p13 chr11: 288,558-695,861 IRF7, TMEM80, 28 more genes
    nsv7058883inversion1nstd229human GRCh38 chr11: 499,565-690,606 , GRCh37.p13 chr11: 499,565-690,606 LOC143666, DEAF1, 13 more genes
    nsv6897314copy number variation1nstd229human GRCh38 chr11: 523,100-528,130 , GRCh37.p13 chr11: 523,100-528,130 LRRC56
    nsv6897071copy number variation1nstd229human GRCh38 chr11: 490,701-585,700 , GRCh37.p13 chr11: 490,701-585,700 MIR210HG, PTDSS2, 9 more genes
    nsv6892374copy number variation1nstd229human GRCh38 chr11: 528,601-530,500 , GRCh37.p13 chr11: 528,601-530,500 HRAS, LRRC56
    nsv6886643copy number variation1nstd229human GRCh38 chr11: 554,813-554,846 , GRCh37.p13 chr11: 554,813-554,846 LMNTD2, LRRC56
    nsv6885572copy number variation1nstd229human GRCh38 chr11: 517,256-561,379 , GRCh37.p13 chr11: 517,256-561,379 RASSF7, HRAS, 3 more genes
    nsv6885001copy number variation1nstd229human GRCh38 chr11: 537,854-551,608 , GRCh37.p13 chr11: 537,854-551,608 LRRC56
    nsv6881074copy number variation1nstd229human GRCh38 chr11: 531,701-535,000 , GRCh37.p13 chr11: 531,701-535,000 LRRC56, HRAS
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6637212copy number variation1nstd102humanPathogenic GRCh37 chr11: 461,373-2,157,956 , GRCh38.p12 chr11: 461,373-2,136,726 MIR6744, PTDSS2, 80 more genes
    nsv6634327copy number variation1nstd102humanPathogenic GRCh38 chr11: 499,700-5,279,697 , GRCh37.p13 chr11: 499,700-5,300,927 SNORA54, PIDD1, 219 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center