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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054915inversion1nstd229human GRCh38 chr5: 72,875,613-72,913,137 , GRCh37.p13 chr5: 72,171,440-72,208,964 RPL35AP13, MIR4804, 1 more genes
    nsv6763618copy number variation1nstd229human GRCh38 chr5: 66,450,908-74,585,645 , GRCh37.p13 chr5: 65,746,736-73,881,470 LOC107986372, LOC105379027, 146 more genes
    nsv6136131copy number variation1nstd213human GRCh37 chr5: 70,130,000-73,760,001 , GRCh38.p12 chr5: 70,834,173-74,464,176 , BTF3, 69 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135435copy number variation1nstd213human GRCh37 chr5: 69,990,000-73,820,001 , GRCh38.p12 chr5: 70,694,173-74,524,176 , BTF3, 71 more genes
    nsv6135198copy number variation1nstd213human GRCh37 chr5: 70,130,000-76,140,001 , GRCh38.p12 chr5: 70,834,173-76,844,176 , BTF3, 117 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
    nsv4455596copy number variation2nstd102humanUncertain significance GRCh37 chr5: 71,721,970-72,431,813 , GRCh38.p12 chr5: 72,426,143-73,135,986 TMEM171, RPL7P22, 10 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
    nsv4333295sequence alteration1nstd166human GRCh37.p13 chr5: 72,112,264-72,508,425 , GRCh38.p12 chr5: 72,816,437-73,212,598 TNPO1, LOC340090, 9 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
    nsv3875351copy number variation1nstd102humanBenign GRCh37 chr5: 72,129,604-72,354,897 , GRCh38.p12 chr5: 72,833,777-73,059,070 TNPO1, MIR4804, 4 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
    nsv2342990short tandem repeat2nstd128human GRCh37 chr5: 72,174,321-72,174,331 , GRCh38.p12 chr5: 72,878,494-72,878,504 TNPO1, RPL35AP13, 1 more genes
    nsv2341621short tandem repeat3nstd128human GRCh37 chr5: 72,174,280-72,174,292 , GRCh38.p12 chr5: 72,878,453-72,878,465 RPL35AP13, MIR4804, 1 more genes
    nsv2341620short tandem repeat3nstd128human GRCh37 chr5: 72,173,977-72,173,993 , GRCh38.p12 chr5: 72,878,150-72,878,166 RPL35AP13, TNPO1, 1 more genes
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