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Items: 15

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    Number of Variants: 15

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3901546copy number variation1nstd102humanPathogenic NCBI36 chr1: 59,057,865-86,336,882 , GRCh37 chr1: 59,285,277-86,564,294 , GRCh38 chr1: 58,819,605-86,098,611 DNASE2B, ROR1, 333 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 DNASE2B, RNA5SP51, 315 more genes
    nsv3886551copy number variation1nstd102humanPathogenic GRCh37 chr1: 64,321,264-88,153,669 , GRCh38.p12 chr1: 63,855,593-87,687,986 DNASE2B, RNU6-1102P, 291 more genes
    nsv3885743copy number variation1nstd102humanPathogenic GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534 DNASE2B, ZNHIT6, 257 more genes
    nsv4454000copy number variation1nstd102humanPathogenic GRCh37 chr1: 67,851,233-86,101,340 , GRCh38.p12 chr1: 67,385,550-85,635,657 DNASE2B, NEXN, 209 more genes
    nsv3905989copy number variation1nstd102humanPathogenic GRCh37 chr1: 76,884,987-89,094,147 , NCBI36 chr1: 76,657,575-88,866,735 , GRCh38 chr1: 76,419,302-88,628,464 DNASE2B, DNAJB4, 146 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 DNASE2B, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 DNASE2B, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 DNASE2B, RNU1-153P, 4887 more genes
    nsv3898327copy number variation1nstd102humanPathogenic GRCh38 chr1: 83,457,325-104,273,917 , GRCh37 chr1: 83,923,008-104,816,539 , NCBI36 chr1: 83,695,596-104,618,062 DNASE2B, LINC01773, 322 more genes
    nsv4728566copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 80,804,502-89,490,384 , GRCh38.p12 chr1: 80,338,817-89,024,701 DNASE2B, CLCA1, 103 more genes
    nsv4450384copy number variation1nstd102humannot provided GRCh37 chr1: 66,085,524-88,429,789 , GRCh38.p12 chr1: 65,619,841-87,964,106 DNASE2B, DEPDC1, 264 more genes
    nsv6313647copy number variation1nstd102humanUncertain significance GRCh37 chr1: 84,084,511-84,921,911 , GRCh38.p12 chr1: 83,618,828-84,456,228 DNASE2B, LINC01725, 7 more genes
    nsv1398038copy number variation1nstd102humanUncertain significance GRCh37 chr1: 84,662,362-85,035,719 , GRCh38.p12 chr1: 84,196,679-84,570,036 DNASE2B, PRKACB, 7 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 DNASE2B, LINC01776, 1853 more genes
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