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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3905689copy number variation1nstd102humanBenign GRCh37 chr11: 40,828,597-40,939,009 , GRCh38.p12 chr11: 40,807,047-40,917,459 LRRC4C
    nsv3902243copy number variation1nstd102humanLikely benign GRCh37 chr11: 40,567,422-40,660,470 , GRCh38.p12 chr11: 40,545,872-40,638,920 LRRC4C
    nsv3901101copy number variation1nstd102humanBenign GRCh37 chr11: 40,794,375-40,854,095 , GRCh38.p12 chr11: 40,772,825-40,832,545 LRRC4C
    nsv3896806copy number variation1nstd102humanBenign GRCh37 chr11: 40,861,418-40,915,339 , GRCh38.p12 chr11: 40,839,868-40,893,789 LRRC4C
    nsv3896208copy number variation1nstd102humanBenign GRCh37 chr11: 41,443,472-41,470,267 , GRCh38.p12 chr11: 41,421,922-41,448,717 LRRC4C
    nsv3923761copy number variation1nstd102humanLikely benign GRCh38 chr11: 40,858,804-41,409,293 , NCBI36 chr11: 40,836,930-41,387,419 , GRCh37 chr11: 40,880,354-41,430,843 LRRC4C, RNU6-365P
    nsv3924266copy number variation1nstd102humanBenign NCBI36 chr11: 40,296,191-40,608,857 , GRCh37 chr11: 40,339,615-40,652,281 , GRCh38 chr11: 40,318,065-40,630,731 LRRC4C, LOC100419712
    nsv3891203copy number variation1nstd102humanBenign GRCh37 chr11: 40,405,192-40,509,532 , GRCh38.p12 chr11: 40,383,642-40,487,982 LRRC4C, LOC100419712
    nsv4729188copy number variation1nstd102humanLikely benign GRCh37 chr11: 40,071,022-40,271,526 , GRCh38.p12 chr11: 40,049,472-40,249,976 LRRC4C, LOC646388
    nsv4455634copy number variation1nstd102humanUncertain significance GRCh37 chr11: 40,829,347-41,488,018 , GRCh38.p12 chr11: 40,807,797-41,466,468 LRRC4C, RNU6-365P
    nsv4675375copy number variation1nstd102humanUncertain significance GRCh37 chr11: 40,831,697-41,487,990 , GRCh38.p12 chr11: 40,810,147-41,466,440 LRRC4C, RNU6-365P
    nsv4675914copy number variation1nstd102humanUncertain significance GRCh37 chr11: 40,888,243-41,323,683 , GRCh38.p12 chr11: 40,866,693-41,302,133 LRRC4C, RNU6-365P
    nsv3905094copy number variation1nstd102humanUncertain significance GRCh37 chr11: 40,191,196-40,555,598 , GRCh38.p12 chr11: 40,169,646-40,534,048 LRRC4C, LOC100419712
    nsv3919080copy number variation1nstd102humanUncertain significance NCBI36 chr11: 40,859,682-41,202,521 , GRCh37.p13 chr11: 40,903,106-41,245,945 , GRCh38.p12 chr11: 40,881,556-41,224,395 LRRC4C, RNU6-365P
    nsv3916722copy number variation1nstd102humanUncertain significance NCBI36 chr11: 40,423,499-40,716,880 , GRCh37 chr11: 40,466,923-40,760,304 , GRCh38 chr11: 40,445,373-40,738,754 LRRC4C, LOC100419712
    nsv3912893copy number variation1nstd102humanUncertain significance NCBI36 chr11: 40,385,553-40,643,925 , GRCh37.p13 chr11: 40,428,977-40,687,349 , GRCh38.p12 chr11: 40,407,427-40,665,799 LRRC4C, LOC100419712
    nsv3906087copy number variation1nstd102humanUncertain significance GRCh37 chr11: 40,453,077-40,654,733 , GRCh38.p12 chr11: 40,431,527-40,633,183 LRRC4C, LOC100419712
    nsv4728927copy number variation1nstd102humanUncertain significance GRCh37 chr11: 40,347,713-40,472,149 , GRCh38.p12 chr11: 40,326,163-40,450,599 LRRC4C, LOC100419712
    nsv3913162copy number variation1nstd102humanUncertain significance GRCh38 chr11: 40,975,875-41,663,216 , GRCh37 chr11: 40,997,425-41,684,766 , NCBI36 chr11: 40,954,001-41,641,342 LRRC4C, LINC02741, 2 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 LRRC4C, FAUP4, 2031 more genes
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