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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5463178copy number variation1nstd206human GRCh38 chr5: 97,073,554-97,201,684 , GRCh37.p13 chr5: 96,409,258-96,537,388 RIOK2, LIX1, 2 more genes
    nsv5456096copy number variation1nstd206human GRCh38 chr5: 97,138,266-97,138,328 , GRCh37.p13 chr5: 96,473,970-96,474,032 LIX1-AS1, LIX1
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4949031copy number variation1nstd200human GRCh38 chr5: 96,412,203-97,185,203 , GRCh37.p13 chr5: 95,747,907-96,520,907 , RNU1-73P, 16 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
    nsv4729594copy number variation1nstd102humanLikely benign GRCh37 chr5: 96,151,759-96,483,691 , GRCh38.p12 chr5: 96,816,056-97,147,987 ERAP2, LIX1, 5 more genes
    nsv4729360copy number variation1nstd102humanUncertain significance GRCh37 chr5: 96,319,606-96,585,510 , GRCh38.p12 chr5: 96,983,902-97,249,806 LNPEP, SETP22, 4 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4675472copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 87,792,844-109,221,844 , GRCh38.p12 chr5: 88,497,027-109,886,143 CAST, CETN3, 202 more genes
    nsv4593356copy number variation2nstd183human GRCh37 chr5: 95,461,836-96,876,792 , GRCh38.p12 chr5: 96,126,132-97,541,088 , ERAP1, 23 more genes
    nsv4591939copy number variation1nstd183human GRCh37 chr5: 96,424,251-96,430,055 , GRCh38.p12 chr5: 97,088,547-97,094,351 LIX1, LIX1-AS1
    nsv4591824copy number variation1nstd183human GRCh37 chr5: 96,428,581-96,429,883 , GRCh38.p12 chr5: 97,092,877-97,094,179 LIX1, LIX1-AS1
    nsv4495713mobile element insertion1nstd166human GRCh37.p13 chr5: 96,442,973-96,442,973 , GRCh38.p12 chr5: 97,107,269-97,107,269 LIX1, LIX1-AS1
    nsv4457189copy number variation1nstd102humanUncertain significance GRCh37 chr5: 96,097,916-96,840,263 , GRCh38.p12 chr5: 96,762,212-97,504,559 LOC100289037, YTHDF1P1, 11 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
    nsv4455828copy number variation1nstd102humanUncertain significance GRCh37 chr5: 95,335,480-97,832,367 , GRCh38.p12 chr5: 95,999,776-98,496,663 LOC107986365, LOC102724070, 32 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
    nsv4328126inversion1nstd166human GRCh37.p13 chr5: 75,669,511-101,876,780 , GRCh38.p12 chr5: 76,373,686-102,541,076 , BHMT, 331 more genes
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