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Items: 1 to 20 of 85

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5681471mobile element insertion1nstd211human GRCh38 chr5: 137,801,082-137,801,082 , GRCh37.p13 chr5: 137,136,771-137,136,771 NPY6R
    nsv5463304copy number variation1nstd206human GRCh38 chr5: 137,810,024-137,816,212 , GRCh37.p13 chr5: 137,145,713-137,151,901 NPY6R
    nsv5454925copy number variation1nstd206human GRCh38 chr5: 137,801,588-137,801,638 , GRCh37.p13 chr5: 137,137,277-137,137,327 NPY6R
    nsv5412429mobile element insertion1nstd206human GRCh38 chr5: 137,801,082-137,801,133 , GRCh37.p13 chr5: 137,136,771-137,136,822 NPY6R
    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
    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
    nsv4938807copy number variation1nstd200human GRCh38 chr5: 137,807,207-137,807,322 , GRCh37.p13 chr5: 137,142,896-137,143,011 NPY6R
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4590171copy number variation1nstd183human GRCh37 chr5: 137,145,649-137,151,748 , GRCh38.p12 chr5: 137,809,960-137,816,059 NPY6R
    nsv4545617insertion1nstd166human GRCh37.p13 chr5: 137,136,705-137,136,705 , GRCh38.p12 chr5: 137,801,016-137,801,016 NPY6R
    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
    nsv4399270copy number variation1nstd174human GRCh37 chr5: 137,121,655-137,137,330 , GRCh38.p12 chr5: 137,785,966-137,801,641 NPY6R
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv3963583copy number variation1nstd168human GRCh38 chr5: 137,809,340-137,856,803 , GRCh37.p13 chr5: 137,145,029-137,192,492 NPY6R, PKD2L2-DT, 1 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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