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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047334inversion1nstd229human GRCh38 chr5: 119,494,072-128,765,801 , GRCh37.p13 chr5: 118,829,767-128,101,494 RPL18P3, KRT18P16, 98 more genes
    nsv7039392inversion1nstd229human GRCh38 chr5: 120,520,478-123,368,624 , GRCh37.p13 chr5: 119,856,173-122,704,318 PPIC-AS1, LOC101927357, 34 more genes
    nsv6761052copy number variation1nstd229human GRCh38 chr5: 123,022,643-123,025,136 , GRCh37.p13 chr5: 122,358,338-122,360,831 SNX24, PPIC, 1 more genes
    nsv6637111copy number variation1nstd102humanPathogenic GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606 SLC12A2, CCDC192, 180 more genes
    nsv6398223copy number variation1nstd223human GRCh38 chr5: 123,022,643-123,025,136 , GRCh37.p13 chr5: 122,358,338-122,360,831 SNX24, RN7SL689P, 1 more genes
    nsv6135380copy number variation1nstd213human GRCh37 chr5: 121,150,000-123,690,001 , GRCh38.p12 chr5: 121,814,305-124,354,308 CSNK1G3, LOX, 34 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6134973copy number variation1nstd213human GRCh37 chr5: 122,220,000-122,390,001 , GRCh38.p12 chr5: 122,884,305-123,054,306 PPIC, SNX24, 2 more genes
    nsv5679348mobile element insertion1nstd211human GRCh38 chr5: 123,022,501-123,022,501 , GRCh37.p13 chr5: 122,358,196-122,358,196 PPIC, SNX24, 1 more genes
    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
    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
    nsv4487680mobile element insertion1nstd166human GRCh37.p13 chr5: 122,366,136-122,366,136 , GRCh38.p12 chr5: 123,030,441-123,030,441 PPIC
    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
    nsv4455632copy number variation1nstd102humanUncertain significance GRCh37 chr5: 120,785,278-122,419,820 , GRCh38.p12 chr5: 121,449,583-123,084,125 FTMT, LOX, 25 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
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