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Items: 11

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    Number of Variants: 11

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 LRRC41, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 LRRC41, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 LRRC41, RNU1-153P, 4887 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LRRC41, LOC107984940, 407 more genes
    nsv3888489copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 45,303,358-52,157,856 , GRCh38.p12 chr1: 44,837,686-51,692,184 LRRC41, CDKN2C, 141 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LRRC41, LINC01776, 1853 more genes
    nsv3889597copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,372,688-47,188,150 , GRCh38.p12 chr1: 45,907,016-46,722,478 LRRC41, NENFP1, 27 more genes
    nsv3882928copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,541,307-47,088,882 , GRCh38.p12 chr1: 46,075,635-46,623,210 LRRC41, PIK3R3, 19 more genes
    nsv3884951copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,747,177-47,280,720 , GRCh38.p12 chr1: 46,281,505-46,815,048 LRRC41, ATPAF1, 19 more genes
    nsv4674638copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,768,408-47,174,149 , GRCh38.p12 chr1: 46,302,736-46,708,477 LRRC41, UQCRH, 17 more genes
    nsv4674480copy number variation1nstd102humanUncertain significance GRCh37 chr1: 46,501,759-46,898,503 , GRCh38.p12 chr1: 46,036,087-46,432,831 LRRC41, TSPAN1, 12 more genes
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