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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
    nsv5362531translocation1nstd200human GRCh38 chr5: 149,403,106-149,403,106 , GRCh38 chr5: 149,402,682-149,402,682 , GRCh37.p13 chr5: 148,782,669-148,782,669 , GRCh37.p13 chr5: 148,782,245-148,782,245 IL17B
    nsv5089269mobile element insertion1nstd203human GRCh38 chr5: 149,372,710-149,372,727 , GRCh37.p13 chr5: 148,752,273-148,752,290 PCYOX1L, IL17B
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4939139copy number variation1nstd200human GRCh38 chr5: 149,369,532-149,375,449 , GRCh37.p13 chr5: 148,749,095-148,755,012 PCYOX1L, IL17B
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4814924copy number variation1nstd200human GRCh37 chr5: 148,782,245-148,782,669 , GRCh38.p12 chr5: 149,402,682-149,403,106 IL17B
    nsv4814923copy number variation1nstd200human GRCh37 chr5: 148,775,008-148,778,202 , GRCh38.p12 chr5: 149,395,445-149,398,639 IL17B
    nsv4814922copy number variation1nstd200human GRCh37 chr5: 148,749,095-148,755,012 , GRCh38.p12 chr5: 149,369,532-149,375,449 PCYOX1L, IL17B
    nsv4457090copy number variation1nstd102humanUncertain significance GRCh37 chr5: 140,424,333-148,985,999 , GRCh38.p12 chr5: 141,044,748-149,606,436 PCDHGC4, CKS1BP5, 165 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
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv4112612copy number variation1nstd166human GRCh37.p13 chr5: 148,773,688-148,773,741 , GRCh38.p12 chr5: 149,394,125-149,394,178 IL17B
    nsv3924856copy number variation1nstd102humanPathogenic NCBI36 chr5: 140,449,756-148,890,434 , GRCh37 chr5: 140,469,572-148,910,241 , GRCh38 chr5: 141,089,988-149,530,678 CTB-99A3.1, C5orf46, 160 more genes
    nsv3923414copy number variation1nstd102humanPathogenic GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811 HNRNPA3P7, RNU6-456P, 514 more genes
    nsv3919840copy number variation1nstd102humanUncertain significance NCBI36 chr5: 148,706,092-148,876,147 , GRCh37.p13 chr5: 148,725,899-148,895,954 , GRCh38.p12 chr5: 149,346,336-149,516,391 CARMN, PCYOX1L, 7 more genes
    nsv3914878copy number variation1nstd102humanPathogenic NCBI36 chr5: 146,520,648-163,194,778 , GRCh37.p13 chr5: 146,540,455-163,262,200 , GRCh38.p12 chr5: 147,160,892-163,835,194 LOC105378231, RN7SKP232, 247 more genes
    nsv3914009copy number variation1nstd102humanPathogenic NCBI36 chr5: 129,211,386-152,713,299 , GRCh38 chr5: 129,847,794-153,353,546 , GRCh37 chr5: 129,183,487-152,733,106 UQCRQ, SNHG4, 489 more genes
    nsv3912937copy number variation1nstd102humanPathogenic GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387 LINC01023, CTB-99A3.1, 783 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
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