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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903839copy number variation1nstd209human GRCh38 chr5: 79,180,365-84,539,350 , GRCh37.p13 chr5: 78,476,188-83,835,168 , ANKRD34B, 84 more genes
    nsv5684546mobile element insertion1nstd211human GRCh38 chr5: 80,630,764-80,630,764 , GRCh37.p13 chr5: 79,926,583-79,926,583 DHFR
    nsv5460412copy number variation1nstd206human GRCh38 chr5: 80,644,758-80,644,862 , GRCh37.p13 chr5: 79,940,577-79,940,681 DHFR
    nsv5381442copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr5: 79,949,868-79,952,360 , GRCh38.p12 chr5: 80,654,049-80,656,541 DHFR, MSH3
    nsv5095359mobile element insertion1nstd203human GRCh38 chr5: 80,640,683-80,640,696 , GRCh37.p13 chr5: 79,936,502-79,936,515 DHFR
    nsv5088088mobile element insertion1nstd203human GRCh38 chr5: 80,637,160-80,637,169 , GRCh37.p13 chr5: 79,932,979-79,932,988 DHFR
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4683856copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr5: 79,949,868-80,171,681 , GRCh38.p12 chr5: 80,654,049-80,875,862 DHFR, MSH3, 1 more genes
    nsv4681453copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,950,537-79,952,360 , GRCh38.p12 chr5: 80,654,718-80,656,541 MSH3, DHFR
    nsv4681240copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,949,868-79,966,138 , GRCh38.p12 chr5: 80,654,049-80,670,319 MSH3, DHFR
    nsv4681043copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr5: 79,949,868-79,974,922 , GRCh38.p12 chr5: 80,654,049-80,679,103 MSH3, DHFR
    nsv4680628copy number variation1nstd189human GRCh37.p13 chr5: 79,720,615-80,127,036 , GRCh38.p12 chr5: 80,424,796-80,831,217 , DBIP2, 9 more genes
    nsv4675820copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,528,733-80,545,287 , GRCh38.p12 chr5: 80,232,914-81,249,468 LINC01337, SERINC5, 23 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4674891copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,705,427-80,237,350 , GRCh38.p12 chr5: 80,409,608-80,941,531 DHFR, FAM151B, 10 more genes
    nsv4665098copy number variation1nstd186human GRCh37 chr5: 79,945,853-79,948,255 , GRCh38.p12 chr5: 80,650,034-80,652,436 DHFR, MTRNR2L2
    nsv4598286copy number variation1nstd183human GRCh37 chr5: 79,922,005-79,925,020 , GRCh38.p12 chr5: 80,626,186-80,629,201 DHFR
    nsv4593282copy number variation1nstd183human GRCh37 chr5: 79,945,853-79,948,255 , GRCh38.p12 chr5: 80,650,034-80,652,436 DHFR, MTRNR2L2
    nsv4591722copy number variation1nstd183human GRCh37 chr5: 79,914,987-79,926,636 , GRCh38.p12 chr5: 80,619,168-80,630,817 LINC01337, DHFR
    nsv4591621copy number variation2nstd183human GRCh37 chr5: 79,945,853-79,948,243 , GRCh38.p12 chr5: 80,650,034-80,652,424 DHFR, MTRNR2L2
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