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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5304523copy number variation1nstd204human GRCh37.p13 chr5: 122,425,969-122,426,085 , GRCh38.p13 chr5: 123,090,274-123,090,390 PRDM6, PRDM6-AS1
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 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
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4738828copy number variation1nstd199human GRCh37 chr5: 122,424,787-122,424,845 , GRCh38.p12 chr5: 123,089,092-123,089,150 PRDM6, PRDM6-AS1
    nsv4675438copy number variation1nstd102humanUncertain significance GRCh37 chr5: 122,143,334-123,430,731 , GRCh38.p12 chr5: 122,807,639-124,095,038 SNX2, KRT18P16, 14 more genes
    nsv4455983copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,949,118-129,317,455 , GRCh38.p12 chr5: 90,653,301-129,981,762 LOC345576, LOC107986436, 419 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
    nsv4345524sequence alteration1nstd166human GRCh37.p13 chr5: 120,941,265-127,230,417 , GRCh38.p12 chr5: 121,605,570-127,894,725 LOX, PPIC, 78 more genes
    nsv4321173inversion1nstd166human GRCh37.p13 chr5: 86,365,040-130,339,409 , GRCh38.p12 chr5: 87,069,223-131,003,716 , APC, 481 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
    nsv4128547copy number variation1nstd166human GRCh37.p13 chr5: 122,406,410-122,471,774 , GRCh38.p12 chr5: 123,070,715-123,136,079 PRDM6, PRDM6-AS1, 2 more genes
    nsv3924205copy number variation1nstd102humanPathogenic GRCh37 chr5: 110,023,143-129,439,531 , GRCh38 chr5: 110,687,442-130,103,838 , NCBI36 chr5: 110,051,042-129,467,430 CSNK1G3, EPB41L4A-AS1, 231 more genes
    nsv3923804copy number variation1nstd102humanPathogenic GRCh37 chr5: 107,644,164-125,113,490 , NCBI36 chr5: 107,672,063-125,141,389 , GRCh38 chr5: 108,308,463-125,777,797 FABP5P6, AP3S1, 202 more genes
    nsv3923717copy number variation1nstd102humanUncertain significance GRCh37 chr5: 121,814,963-126,168,860 , GRCh38 chr5: 122,479,268-126,833,168 , NCBI36 chr5: 121,842,862-126,196,759 RN7SL689P, HSPE1P10, 49 more genes
    nsv3921962copy number variation1nstd102humanPathogenic GRCh38 chr5: 114,707,561-126,507,744 , NCBI36 chr5: 114,071,157-125,871,335 , GRCh37 chr5: 114,043,258-125,843,436 RNU2-49P, LINC02240, 139 more genes
    nsv3919087copy number variation1nstd102humanPathogenic GRCh38 chr5: 120,739,630-126,823,984 , NCBI36 chr5: 120,103,224-126,187,575 , GRCh37 chr5: 120,075,325-126,159,676 KRT8P33, LOC107986448, 67 more genes
    nsv3916468copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,670,423-127,412,115 , GRCh38 chr5: 90,374,606-128,076,423 , NCBI36 chr5: 89,706,179-127,440,014 LOC105379149, LOC107986365, 406 more genes
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