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Items: 11

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    Number of Variants: 11

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3887381copy number variation1nstd102humanBenign GRCh37 chr1: 53,542,620-53,553,754 , GRCh38.p12 chr1: 53,076,948-53,088,082 PODN, SLC1A7
    nsv5381135copy number variation1nstd102humanPathogenic GRCh37 chr1: 51,941,877-56,688,514 , GRCh38.p12 chr1: 51,476,205-56,222,842 PODN, LRP8-DT, 122 more genes
    nsv3871136copy number variation1nstd102humanPathogenic GRCh37 chr1: 51,729,573-55,164,001 , GRCh38.p12 chr1: 51,263,901-54,698,328 PODN, MROH7, 100 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 PODN, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 PODN, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 PODN, RNU1-153P, 4887 more genes
    nsv3896927copy number variation1nstd102humanPathogenic GRCh37 chr1: 53,061,024-77,233,450 , GRCh38 chr1: 52,595,352-76,767,765 , NCBI36 chr1: 52,833,612-77,006,038 PODN, DNAI4, 346 more genes
    nsv3899721copy number variation1nstd102humanLikely pathogenic NCBI36 chr1: 53,025,763-67,578,144 , GRCh37 chr1: 53,253,175-67,805,556 , GRCh38 chr1: 52,787,503-67,339,873 PODN, AK4, 230 more genes
    nsv4674651copy number variation1nstd102humanLikely benign GRCh37 chr1: 53,039,602-53,734,721 , GRCh38.p12 chr1: 52,573,930-53,269,049 PODN, TUBBP10, 27 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 PODN, LINC01776, 1853 more genes
    nsv3888039copy number variation1nstd102humanUncertain significance GRCh37 chr1: 53,370,010-54,017,544 , GRCh38.p12 chr1: 52,904,338-53,551,871 PODN, LOC105378731, 24 more genes
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