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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5685379mobile element insertion2nstd211human GRCh38 chr5: 138,437,404-138,437,404 , GRCh37.p13 chr5: 137,773,093-137,773,093 REEP2, KDM3B
    nsv5401177mobile element insertion1nstd206human GRCh38 chr5: 138,437,404-138,437,455 , GRCh37.p13 chr5: 137,773,093-137,773,144 REEP2, KDM3B
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5083043mobile element insertion1nstd203human GRCh38 chr5: 138,437,388-138,437,401 , GRCh37.p13 chr5: 137,773,077-137,773,090 REEP2, KDM3B
    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
    nsv4804144copy number variation1nstd200human GRCh37 chr5: 137,782,901-137,783,192 , GRCh38.p12 chr5: 138,447,212-138,447,503 REEP2
    nsv4769371copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 137,754,277-138,994,590 , GRCh38.p12 chr5: 138,418,588-139,615,005 CTNNA1, EGR1, 36 more genes
    nsv4493207mobile element insertion1nstd166human GRCh37.p13 chr5: 137,773,077-137,773,077 , GRCh38.p12 chr5: 138,437,388-138,437,388 KDM3B, REEP2
    nsv4493164mobile element insertion1nstd166human GRCh37.p13 chr5: 137,776,356-137,776,356 , GRCh38.p12 chr5: 138,440,667-138,440,667 REEP2
    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
    nsv3924452copy number variation1nstd102humanUncertain significance GRCh37 chr5: 137,515,583-138,375,579 , GRCh38 chr5: 138,179,894-139,039,890 , NCBI36 chr5: 137,543,482-138,403,478 HSPA9, CDC23, 21 more genes
    nsv3923450copy number variation1nstd102humanPathogenic GRCh37 chr5: 137,172,371-140,075,946 , NCBI36 chr5: 137,200,270-140,056,130 , GRCh38 chr5: 137,836,682-140,696,361 RNU6-236P, FAM13B, 89 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
    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
    nsv3910250copy number variation1nstd102humanPathogenic GRCh38 chr5: 135,297,294-140,106,003 , GRCh37 chr5: 134,632,984-139,485,588 , NCBI36 chr5: 134,660,883-139,465,772 SNORD63, HSPA9, 94 more genes
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