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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3877988copy number variation1nstd102humanBenign GRCh37 chr1: 86,296,663-86,297,495 , GRCh38.p12 chr1: 85,830,980-85,831,812 COL24A1
    nsv4728650copy number variation1nstd102humanLikely benign GRCh37 chr1: 86,225,155-86,392,069 , GRCh38.p12 chr1: 85,759,472-85,926,386 COL24A1, RNA5SP51
    nsv6290529copy number variation1nstd102humanLikely benign GRCh37 chr1: 86,225,155-86,387,725 , GRCh38.p12 chr1: 85,759,472-85,922,042 COL24A1, RNA5SP51
    nsv3878606copy number variation1nstd102humanBenign GRCh37 chr1: 86,229,604-86,384,082 , GRCh38.p12 chr1: 85,763,921-85,918,399 COL24A1, RNA5SP51
    nsv3872992copy number variation1nstd102humanBenign GRCh37 chr1: 86,233,871-86,384,082 , GRCh38.p12 chr1: 85,768,188-85,918,399 COL24A1, RNA5SP51
    nsv3904449copy number variation1nstd102humanLikely benign NCBI36 chr1: 85,900,439-86,431,014 , GRCh37 chr1: 86,127,851-86,658,426 , GRCh38 chr1: 85,662,168-86,192,743 COL24A1, LOC105378823, 2 more genes
    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 COL24A1, ROR1, 333 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 COL24A1, RNA5SP51, 315 more genes
    nsv3886551copy number variation1nstd102humanPathogenic GRCh37 chr1: 64,321,264-88,153,669 , GRCh38.p12 chr1: 63,855,593-87,687,986 COL24A1, 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 COL24A1, ZNHIT6, 257 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 COL24A1, DNAJB4, 146 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 COL24A1, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 COL24A1, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 COL24A1, 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 COL24A1, 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 COL24A1, CLCA1, 103 more genes
    nsv3871671copy number variation1nstd102humanBenign GRCh37 chr1: 85,765,619-86,697,145 , GRCh38.p12 chr1: 85,299,936-86,231,462 COL24A1, CCN1, 6 more genes
    nsv3882306copy number variation1nstd102humanLikely benign GRCh37 chr1: 86,006,704-86,727,751 , GRCh38.p12 chr1: 85,541,021-86,262,068 COL24A1, DDAH1, 6 more genes
    nsv4728696copy number variation1nstd102humanLikely benign GRCh37 chr1: 86,441,405-86,925,675 , GRCh38.p12 chr1: 85,975,722-86,459,992 COL24A1, ODF2L, 5 more genes
    nsv3882974copy number variation2nstd102humanUncertain significance GRCh37 chr1: 85,761,564-86,703,902 , GRCh38.p12 chr1: 85,295,881-86,238,219 COL24A1, RNA5SP51, 6 more genes
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