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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5471050copy number variation1nstd206human GRCh38 chr5: 137,856,777-138,124,570 , GRCh37.p13 chr5: 137,192,466-137,460,259 RNU6-460P, RNU6-1148P, 9 more genes
    nsv5461369copy number variation1nstd206human GRCh38 chr5: 138,028,983-138,032,411 , GRCh37.p13 chr5: 137,364,672-137,368,100 FAM13B-AS1, FAM13B
    nsv5381777copy number variation1nstd102humanPathogenic GRCh37 chr5: 136,409,875-137,739,167 , GRCh38.p12 chr5: 137,074,186-138,403,478 HNRNPA0, SPOCK1, 24 more genes
    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
    nsv5302092copy number variation1nstd204human GRCh38.p13 chr5: 137,856,772-138,124,571 , GRCh37.p13 chr5: 137,192,461-137,460,260 RNU6-1148P, PKD2L2-DT, 9 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
    nsv4945115copy number variation1nstd200human GRCh38 chr5: 137,856,777-138,124,570 , GRCh37.p13 chr5: 137,192,466-137,460,259 RNU6-1148P, FAM13B, 9 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4805850copy number variation1nstd200human GRCh37 chr5: 137,192,466-137,460,259 , GRCh38.p12 chr5: 137,856,777-138,124,570 RNU6-888P, PKD2L2, 9 more genes
    nsv4590172copy number variation1nstd183human GRCh37 chr5: 137,368,461-137,368,685 , GRCh38.p12 chr5: 138,032,772-138,032,996 FAM13B-AS1, FAM13B
    nsv4552511insertion1nstd166human GRCh37.p13 chr5: 137,373,342-137,373,342 , GRCh38.p12 chr5: 138,037,653-138,037,653 FAM13B-AS1, FAM13B
    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
    nsv3967646copy number variation1nstd168human GRCh37.p13 chr5: 137,181,447-137,422,300 , GRCh38 chr5: 137,845,758-138,086,611 WNT8A, MYOT, 6 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
    nsv3919979copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,737,257-137,772,727 , GRCh38 chr5: 133,401,565-138,437,038 , NCBI36 chr5: 132,765,156-137,800,626 FBXL21P, MIR5692C1, 92 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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