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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4682168copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 150,658,258-150,663,476 , GRCh38.p12 chr3: 150,940,471-150,945,689 CLRN1
    nsv6313477copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,641,476-150,665,244 , GRCh38.p12 chr3: 150,923,689-150,947,457 CLRN1
    nsv4454990copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,647,395-150,665,244 , GRCh38.p12 chr3: 150,929,608-150,947,457 CLRN1
    nsv4454602copy number variation1nstd102humanPathogenic GRCh37 chr3: 150,690,233-150,690,796 , GRCh38 chr3: 150,972,446-150,973,009 CLRN1, CLRN1-AS1
    nsv3919564copy number variation1nstd102humanUncertain significance NCBI36 chr3: 152,254,568-152,382,804 , GRCh37.p13 chr3: 150,771,878-150,900,114 , GRCh38.p12 chr3: 151,054,091-151,182,327 MED12L, CLRN1-AS1
    nsv6311959copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,645,723-150,690,495 , GRCh38.p12 chr3: 150,927,936-150,972,708 CLRN1, CLRN1-AS1
    nsv3915058copy number variation1nstd102humanLikely benign GRCh37 chr3: 150,607,390-150,860,207 , NCBI36 chr3: 152,090,080-152,342,897 , GRCh38 chr3: 150,889,603-151,142,420 CLRN1, MED12L, 2 more genes
    nsv6636735copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,534,296-150,908,849 , GRCh38.p12 chr3: 150,816,509-151,191,062 CLRN1, MINDY4B, 3 more genes
    nsv6636766copy number variation1nstd102humanUncertain significance GRCh37 chr3: 150,546,825-150,878,912 , GRCh38.p12 chr3: 150,829,038-151,161,125 CLRN1, MINDY4B, 2 more genes
    nsv6314533complex chromosomal rearrangement3nstd102humanUncertain significance GRCh37 chr3: 150,641,974-150,641,974 , GRCh37 chr3: 150,641,979-150,641,979 , GRCh38.p12 chr3: 150,924,187-150,924,187 , GRCh38.p12 chr3: 150,924,192-150,924,192 , GRCh38.p12 chr1: 72,057,442-72,057,442 , GRCh38.p12 chr1: 72,057,444-72,057,444 , GRCh38.p12 chr1: 72,474,628-72,474,628 , GRCh38.p12 chr1: 72,474,630-72,474,630 , GRCh37 chr1: 72,523,125-72,523,125 , GRCh37 chr1: 72,523,127-72,523,127 , GRCh37 chr1: 72,940,311-72,940,311 , GRCh37 chr1: 72,940,313-72,940,313 CLRN1, NEGR1, 1 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 CLRN1, LOC102724145, 273 more genes
    nsv3887637copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,425,748-153,220,169 , GRCh38.p12 chr3: 148,707,961-153,502,380 CLRN1, LOC101927942, 97 more genes
    nsv4674301copy number variation1nstd102humanPathogenic GRCh37 chr3: 149,404,255-152,786,331 , GRCh38.p12 chr3: 149,686,468-153,068,542 CLRN1, EIF3JP2, 63 more genes
    nsv6311444copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,447,967-151,176,497 , GRCh38.p12 chr3: 148,730,180-151,458,709 CLRN1, TM4SF1, 68 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 CLRN1, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 CLRN1, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 CLRN1, RPL23AP49, 2875 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 CLRN1, LINC02614, 1469 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 CLRN1, H1-10, 846 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 CLRN1, LOC105374179, 785 more genes
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