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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4591583copy number variation1nstd183human GRCh37 chr5: 72,733,703-72,836,482 , GRCh38.p12 chr5: 73,437,876-73,540,657 FOXD1, LINC01386, 2 more genes
    nsv4578696copy number variation1nstd102humanLikely pathogenic GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205 TRIM23, BTF3, 215 more genes
    nsv4547513insertion1nstd166human GRCh37.p13 chr5: 72,796,932-72,796,932 , GRCh38.p12 chr5: 73,501,107-73,501,107 BTF3
    nsv4540041insertion1nstd166human GRCh37.p13 chr5: 72,796,794-72,796,794 , GRCh38.p12 chr5: 73,500,969-73,500,969 BTF3
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3911585copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550 LINC02241, ATPSCKMT, 878 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 SPEF2, NDST1, 2490 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 PCDHGC5, RGS14, 2492 more genes
    nsv3133656copy number variation2nstd151human GRCh37 chr5: 72,801,014-72,801,068 , GRCh38.p12 chr5: 73,505,189-73,505,243 BTF3
    nsv2343063short tandem repeat1nstd128human GRCh37 chr5: 72,800,473-72,800,484 , GRCh38.p12 chr5: 73,504,648-73,504,659 BTF3
    nsv2342411short tandem repeat1nstd128human GRCh37 chr5: 72,792,733-72,792,751 , GRCh38.p12 chr5: 73,496,908-73,496,926 BTF3
    nsv2342269short tandem repeat3nstd128human GRCh37 chr5: 72,800,864-72,800,877 , GRCh38.p12 chr5: 73,505,039-73,505,052 BTF3
    nsv2340268short tandem repeat4nstd128human GRCh37 chr5: 72,798,503-72,798,516 , GRCh38.p12 chr5: 73,502,678-73,502,691 BTF3
    nsv2340267short tandem repeat5nstd128human GRCh37 chr5: 72,796,755-72,796,769 , GRCh38.p12 chr5: 73,500,930-73,500,944 BTF3
    esv3815459copy number variation1estd192human GRCh37 chr5: 55,448,215-119,510,134 , GRCh38.p12 chr5: 56,152,388-120,174,439 , LOC105379138, 829 more genes
    esv3803325copy number variation1estd192human GRCh37 chr5: 55,814,376-95,636,328 , GRCh38.p12 chr5: 56,518,549-96,300,624 , LOC100130001, 560 more genes
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