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Items: 1 to 20 of 26

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3872134copy number variation1nstd102humanLikely benign GRCh37 chr1: 76,255,060-76,259,801 , GRCh38.p12 chr1: 75,789,375-75,794,116 RABGGTB, SNORD45B
    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 RABGGTB, ROR1, 333 more genes
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RABGGTB, RNA5SP51, 315 more genes
    nsv3886551copy number variation1nstd102humanPathogenic GRCh37 chr1: 64,321,264-88,153,669 , GRCh38.p12 chr1: 63,855,593-87,687,986 RABGGTB, 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 RABGGTB, ZNHIT6, 257 more genes
    nsv4454000copy number variation1nstd102humanPathogenic GRCh37 chr1: 67,851,233-86,101,340 , GRCh38.p12 chr1: 67,385,550-85,635,657 RABGGTB, NEXN, 209 more genes
    nsv3884583copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,351,024-79,583,933 , GRCh38.p12 chr1: 60,885,352-79,118,248 RABGGTB, MIR7156, 243 more genes
    nsv3903468copy number variation1nstd102humanPathogenic NCBI36 chr1: 59,870,760-76,969,150 , GRCh37 chr1: 60,098,172-77,196,562 , GRCh38 chr1: 59,632,500-76,730,877 RABGGTB, WLS, 219 more genes
    nsv3908260copy number variation1nstd102humanPathogenic GRCh37 chr1: 67,330,808-77,589,066 , NCBI36 chr1: 67,103,396-77,361,654 , GRCh38 chr1: 66,865,125-77,123,381 RABGGTB, RNA5SP50, 119 more genes
    nsv4449847copy number variation1nstd102humanPathogenic GRCh37 chr1: 66,868,168-77,106,425 , GRCh38.p12 chr1: 66,402,485-76,640,740 RABGGTB, GNG12-AS1, 118 more genes
    nsv3883042copy number variation1nstd102humanPathogenic GRCh37 chr1: 76,007,120-76,540,569 , GRCh38 chr1: 75,541,435-76,074,884 RABGGTB, ACADM, 12 more genes
    nsv3877365copy number variation1nstd102humanPathogenic GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250 RABGGTB, MARK1, 4930 more genes
    nsv3885206copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793 RABGGTB, SNAP47, 4927 more genes
    nsv3884414copy number variation2nstd102humanPathogenic GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485 RABGGTB, 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 RABGGTB, DNAI4, 346 more genes
    nsv4347043copy number variation1nstd102humanPathogenic GRCh37 chr1: 71,410,579-78,131,158 , GRCh38.p12 chr1: 70,944,896-77,665,473 RABGGTB, ST6GALNAC3, 67 more genes
    nsv3876937copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 75,648,797-77,770,044 , GRCh38.p12 chr1: 75,183,112-77,304,359 RABGGTB, ACADM, 28 more genes
    nsv3887757copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 72,103,442-77,186,974 , GRCh38.p12 chr1: 71,637,759-76,721,289 RABGGTB, ACADM, 48 more genes
    nsv3882379copy number variation1nstd102humanBenign GRCh37 chr1: 76,177,994-76,311,291 , GRCh38.p12 chr1: 75,712,309-75,845,606 RABGGTB, ACADM, 6 more genes
    nsv3876095copy number variation1nstd102humanLikely benign GRCh37 chr1: 76,050,176-76,623,228 , GRCh38.p12 chr1: 75,584,491-76,157,543 RABGGTB, DLSTP1, 11 more genes
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