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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3907967copy number variation1nstd102humanUncertain significance NCBI36 chr1: 242,876,771-242,898,413 , GRCh38 chr1: 244,646,846-244,668,488 , GRCh37 chr1: 244,810,148-244,831,790 DESI2
    nsv3882300copy number variation1nstd102humanLikely benign GRCh37 chr1: 244,632,254-244,851,134 , GRCh38.p12 chr1: 244,468,952-244,687,832 DESI2, CYCSP5, 1 more genes
    nsv6634337copy number variation1nstd102humanPathogenic GRCh37 chr1: 233,012,994-249,206,918 , GRCh38.p12 chr1: 232,877,248-248,912,719 DESI2, OR2M4, 316 more genes
    nsv3876145copy number variation1nstd102humanPathogenic GRCh37 chr1: 235,797,384-249,224,684 , GRCh38.p12 chr1: 235,634,084-248,930,485 DESI2, OR11L1, 257 more genes
    nsv3893126copy number variation1nstd102humanPathogenic GRCh37 chr1: 236,719,382-249,212,668 , GRCh38 chr1: 236,556,082-248,918,469 , NCBI36 chr1: 234,786,005-247,179,291 DESI2, RNU6-1205P, 239 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 DESI2, RNU6-747P, 172 more genes
    nsv3895463copy number variation1nstd102humanPathogenic GRCh37 chr1: 237,806,581-249,212,668 , NCBI36 chr1: 235,873,204-247,179,291 , GRCh38 chr1: 237,643,281-248,918,469 DESI2, RPL37P8, 229 more genes
    nsv3906971copy number variation1nstd102humanPathogenic GRCh38 chr1: 238,033,575-248,924,534 , GRCh37 chr1: 238,196,875-249,218,733 , NCBI36 chr1: 236,263,498-247,185,356 DESI2, RNU1-132P, 217 more genes
    nsv3908875copy number variation1nstd102humanPathogenic GRCh37 chr1: 238,356,180-249,224,684 , NCBI36 chr1: 236,422,803-247,191,307 , GRCh38 chr1: 238,192,880-248,930,485 DESI2, ZNF124, 216 more genes
    nsv3892441copy number variation1nstd102humanPathogenic NCBI36 chr1: 236,581,044-247,179,291 , GRCh38 chr1: 238,351,121-248,918,469 , GRCh37 chr1: 238,514,421-249,212,668 DESI2, SH3BP5L, 215 more genes
    nsv3906180copy number variation1nstd102humanPathogenic GRCh38 chr1: 238,753,749-248,918,467 , NCBI36 chr1: 236,983,672-247,179,289 , GRCh37 chr1: 238,917,049-249,212,666 DESI2, ZNF496, 212 more genes
    nsv3896965copy number variation1nstd102humanPathogenic GRCh37 chr1: 239,721,730-249,212,668 , GRCh38 chr1: 239,558,430-248,918,469 , NCBI36 chr1: 237,788,353-247,179,291 DESI2, OR14I1, 208 more genes
    nsv3905218copy number variation1nstd102humanPathogenic NCBI36 chr1: 237,859,791-247,185,415 , GRCh37 chr1: 239,793,168-249,218,792 , GRCh38 chr1: 239,629,868-248,924,593 DESI2, RSL24D1P4, 208 more genes
    nsv6636648copy number variation1nstd102humanPathogenic GRCh37 chr1: 239,910,960-249,224,684 , GRCh38.p12 chr1: 239,747,660-248,930,485 DESI2, RFKP1, 206 more genes
    nsv3893822copy number variation1nstd102humanPathogenic GRCh38 chr1: 240,465,122-248,918,469 , NCBI36 chr1: 238,695,045-247,179,291 , GRCh37 chr1: 240,628,422-249,212,668 DESI2, RSL24D1P4, 199 more genes
    nsv3880927copy number variation1nstd102humanPathogenic GRCh37 chr1: 241,051,170-249,224,684 , GRCh38.p12 chr1: 240,887,870-248,930,485 DESI2, LOC105373249, 190 more genes
    nsv3903138copy number variation1nstd102humanPathogenic GRCh38 chr1: 241,047,422-248,924,593 , GRCh37 chr1: 241,210,722-249,218,792 , NCBI36 chr1: 239,277,345-247,185,415 DESI2, LOC343165, 188 more genes
    nsv3892072copy number variation1nstd102humanPathogenic NCBI36 chr1: 239,987,174-247,152,131 , GRCh37 chr1: 241,920,551-249,185,508 , GRCh38 chr1: 241,757,249-248,891,309 DESI2, VN1R17P, 180 more genes
    nsv3889989copy number variation1nstd102humanPathogenic GRCh37 chr1: 240,620,284-247,690,417 , GRCh38.p12 chr1: 240,456,984-247,527,115 DESI2, LOC107985725, 124 more genes
    nsv3891199copy number variation1nstd102humanPathogenic NCBI36 chr1: 240,275,204-247,191,307 , GRCh38 chr1: 242,045,279-248,930,485 , GRCh37 chr1: 242,208,581-249,224,684 DESI2, OR2T33, 172 more genes
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