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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5629503insertion1nstd207human GRCh38 chr5: 147,837,649-147,837,649 , GRCh37.p13 chr5: 147,217,212-147,217,212 SPINK1
    nsv5306956copy number variation1nstd204human GRCh37.p13 chr5: 147,100,941-147,326,822 , GRCh38.p13 chr5: 147,721,378-147,947,259 SPINK1, JAKMIP2, 5 more genes
    nsv5227548copy number variation1nstd204human GRCh37.p13 chr5: 147,101,964-147,325,463 , GRCh38.p13 chr5: 147,722,401-147,945,900 SPINK1, JAKMIP2, 5 more genes
    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
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4760500insertion1nstd199human GRCh37 chr5: 147,217,222-147,217,222 , GRCh38.p12 chr5: 147,837,659-147,837,659 SPINK1
    nsv4728780copy number variation1nstd102humanUncertain significance GRCh37 chr5: 147,088,554-147,321,173 , GRCh38.p12 chr5: 147,708,991-147,941,610 SPINK1, LOC105378218, 5 more genes
    nsv4682804copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr5: 147,204,224-147,211,355 , GRCh38.p12 chr5: 147,824,661-147,831,792 SPINK1
    nsv4483000mobile element insertion1nstd166human GRCh37.p13 chr5: 147,202,178-147,202,178 , GRCh38.p12 chr5: 147,822,615-147,822,615 SPINK1
    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
    nsv4383807copy number variation1nstd173human GRCh37 chr5: 147,105,067-147,321,173 , GRCh38.p12 chr5: 147,725,504-147,941,610 C5orf46, EEF1GP2, 5 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
    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
    nsv3918033copy number variation1nstd102humanPathogenic GRCh38 chr5: 145,197,355-148,541,511 , NCBI36 chr5: 144,557,111-147,901,267 , GRCh37 chr5: 144,576,918-147,921,074 LOC100288484, PRELID3BP9, 50 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
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