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Items: 1 to 20 of 643

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148265copy number variation1nstd102humanPathogenic GRCh38 chr5: 176,447,531-177,312,407 , GRCh37.p13 chr5: 175,874,532-176,739,408 MXD3, FAF2, 19 more genes
    nsv7097523copy number variation2nstd102humanPathogenic GRCh37 chr5: 176,289,625-177,151,363 , GRCh38.p12 chr5: 176,862,624-177,724,362 PFN3, DBN1, 29 more genes
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7096768copy number variation1nstd102humanPathogenic GRCh37 chr5: 176,720,813-176,722,460 , GRCh38.p12 chr5: 177,293,812-177,295,459 NSD1
    nsv7096767copy number variation1nstd102humanUncertain significance GRCh37 chr5: 176,618,865-177,036,696 , GRCh38.p12 chr5: 177,191,864-177,609,695 PFN3, NSD1, 21 more genes
    nsv7093520insertion1nstd102humanPathogenic GRCh37 chr5: 176,687,126-176,687,126 , GRCh38 chr5: 177,260,125-177,260,125 NSD1
    nsv7055858inversion1nstd229human GRCh38 chr5: 177,223,586-177,230,157 , GRCh37.p13 chr5: 176,650,587-176,657,158 NSD1
    nsv7050002inversion1nstd229human GRCh38 chr5: 175,906,338-177,936,522 , GRCh37.p13 chr5: 175,333,341-177,363,523 PRR7, OR1X5P, 60 more genes
    nsv7041943inversion1nstd229human GRCh38 chr5: 176,986,483-178,673,578 , GRCh37.p13 chr5: 176,413,484-178,100,579 DBN1, LOC100419951, 54 more genes
    nsv7041901inversion1nstd229human GRCh38 chr5: 175,920,087-179,128,938 , GRCh37.p13 chr5: 175,347,090-178,555,939 LOC100288803, NHP2, 98 more genes
    nsv7040659inversion1nstd229human GRCh38 chr5: 174,927,732-178,443,561 , GRCh37.p13 chr5: 174,354,735-177,870,562 RN7SKP148, FAM193B-DT, 90 more genes
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv7038147inversion1nstd229human GRCh38 chr5: 177,229,442-177,234,162 , GRCh37.p13 chr5: 176,656,443-176,661,163 NSD1
    nsv6797828copy number variation1nstd229human GRCh38 chr5: 177,152,284-177,154,975 , GRCh37.p13 chr5: 176,579,285-176,581,976 NSD1
    nsv6796327copy number variation1nstd229human GRCh38 chr5: 177,219,684-177,226,761 , GRCh37.p13 chr5: 176,646,685-176,653,762 NSD1
    nsv6795968copy number variation1nstd229human GRCh38 chr5: 177,216,771-177,222,278 , GRCh37.p13 chr5: 176,643,772-176,649,279 NSD1
    nsv6795218copy number variation1nstd229human GRCh38 chr5: 177,175,486-177,180,116 , GRCh37.p13 chr5: 176,602,487-176,607,117 NSD1
    nsv6795042copy number variation1nstd229human GRCh38 chr5: 177,140,944-177,154,944 , GRCh37.p13 chr5: 176,567,945-176,581,945 NSD1
    nsv6794262copy number variation1nstd229human GRCh38 chr5: 177,164,814-177,173,770 , GRCh37.p13 chr5: 176,591,815-176,600,771 NSD1
    nsv6790441copy number variation1nstd229human GRCh38 chr5: 177,272,781-177,273,414 , GRCh37.p13 chr5: 176,699,782-176,700,415 NSD1
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