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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901287copy number variation1nstd209human GRCh38 chr5: 141,632,244-142,199,968 , GRCh37.p13 chr5: 141,011,811-141,579,533 LOC107986454, NDFIP1, 13 more genes
    nsv5894078copy number variation1nstd209human GRCh38 chr5: 141,632,148-142,199,870 , GRCh37.p13 chr5: 141,011,715-141,579,435 DELE1, LOC729080, 13 more genes
    nsv5691005mobile element insertion1nstd211human GRCh38 chr5: 141,635,993-141,635,993 , GRCh37.p13 chr5: 141,015,560-141,015,560 RELL2, HDAC3
    nsv5407979mobile element insertion1nstd206human GRCh38 chr5: 141,635,993-141,636,018 , GRCh37.p13 chr5: 141,015,560-141,015,585 HDAC3, RELL2
    nsv5098094mobile element insertion1nstd203human GRCh38 chr5: 141,635,983-141,635,993 , GRCh37.p13 chr5: 141,015,550-141,015,560 RELL2, HDAC3
    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
    nsv4804238copy number variation1nstd200human GRCh37 chr5: 141,015,268-141,015,636 , GRCh38.p12 chr5: 141,635,701-141,636,069 RELL2, HDAC3
    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
    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
    nsv3924309copy number variation1nstd102humanPathogenic GRCh37 chr5: 138,206,826-145,191,872 , GRCh38 chr5: 138,871,137-145,812,309 , NCBI36 chr5: 138,234,725-145,172,065 FCHSD1, LOC105378208, 183 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
    nsv3918788copy number variation1nstd102humanUncertain significance NCBI36 chr5: 140,322,968-141,682,547 , GRCh38 chr5: 140,963,199-142,322,798 , GRCh37 chr5: 140,453,735-141,702,363 PCDHB2, PCDHGA5, 86 more genes
    nsv3915613copy number variation1nstd102humanUncertain significance NCBI36 chr5: 140,977,574-141,222,391 , GRCh37.p13 chr5: 140,997,390-141,242,207 , GRCh38.p12 chr5: 141,617,823-141,862,642 RELL2, ARAP3, 5 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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