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Items: 1 to 20 of 68

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5094141mobile element insertion1nstd203human GRCh38 chr5: 55,166,675-55,166,689 , GRCh37.p13 chr5: 54,462,503-54,462,517 CDC20B, GPX8
    nsv4451131copy number variation1nstd102humanUncertain significance GRCh37 chr5: 53,180,658-54,552,379 , GRCh38.p12 chr5: 53,884,828-55,256,551 HSPB3, LOC102467081, 25 more genes
    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
    nsv4119813copy number variation1nstd166human GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790 , ESM1, 305 more genes
    nsv3923429copy number variation1nstd102humanPathogenic GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770 ISCA1P1, LOC643307, 163 more genes
    nsv3922909copy number variation1nstd102humanPathogenic GRCh38 chr5: 50,462,100-55,862,985 , GRCh37 chr5: 49,757,934-55,158,813 , NCBI36 chr5: 49,793,691-55,194,570 HMGB1P47, ITGA1, 72 more genes
    nsv3920391copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725 KRT18P56, LINC01265, 290 more genes
    nsv3917640copy number variation1nstd102humanUncertain significance NCBI36 chr5: 54,359,842-55,271,282 , GRCh38 chr5: 55,028,257-55,939,697 , GRCh37 chr5: 54,324,085-55,235,525 MIR449C, GPX8, 24 more genes
    nsv3913817copy number variation1nstd102humanUncertain significance GRCh37 chr5: 45,566,963-55,802,320 , GRCh38 chr5: 45,566,861-56,506,493 , NCBI36 chr5: 45,602,720-55,838,077 LINC02118, ARL15, 90 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
    nsv3878755copy number variation1nstd102humanLikely benign GRCh37 chr5: 53,784,524-54,985,838 , GRCh38.p12 chr5: 54,488,694-55,690,010 MIR449C, ESM1, 26 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
    nsv3130747copy number variation1nstd151human GRCh37 chr5: 54,429,237-54,558,765 , GRCh38.p12 chr5: 55,133,409-55,262,937 CCNO, MCIDAS, 6 more genes
    nsv3127420copy number variation1nstd151human GRCh37 chr5: 54,436,139-54,558,765 , GRCh38.p12 chr5: 55,140,311-55,262,937 DHX29, CDC20B, 6 more genes
    esv4010710copy number variation1estd233human GRCh37 chr5: 49,560,000-66,066,000 , GRCh38.p12 chr5: 50,264,166-66,770,172 , TRIM23, 208 more genes
    nsv2333662short tandem repeat1nstd128human GRCh37 chr5: 54,458,222-54,458,237 , GRCh38.p12 chr5: 55,162,394-55,162,409 GPX8, CDC20B
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