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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4949026copy number variation1nstd200human GRCh38 chr5: 94,559,553-95,742,662 , GRCh37.p13 chr5: 93,895,258-95,078,366 , ARSK, 20 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
    nsv4676056copy number variation1nstd102humanUncertain significance GRCh37 chr5: 94,952,542-95,069,744 , GRCh38.p12 chr5: 95,616,838-95,734,040 RHOBTB3, SPATA9, 4 more genes
    nsv4675889copy number variation1nstd102humanUncertain significance GRCh37 chr5: 94,715,085-95,251,238 , GRCh38.p12 chr5: 95,379,381-95,915,534 RHOBTB3, ELL2, 17 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
    nsv4593354copy number variation1nstd183human GRCh37 chr5: 94,956,255-94,956,882 , GRCh38.p12 chr5: 95,620,551-95,621,178 LOC112267933, GPR150
    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
    nsv4405996copy number variation1nstd174human GRCh37 chr5: 94,956,239-94,956,904 , GRCh38.p12 chr5: 95,620,535-95,621,200 LOC112267933, GPR150
    nsv4398339copy number variation1nstd174human GRCh37 chr5: 94,955,602-94,957,264 , GRCh38.p12 chr5: 95,619,898-95,621,560 GPR150, LOC112267933
    nsv4380528copy number variation2nstd173human GRCh37 chr5: 94,958,290-94,991,346 , GRCh38.p12 chr5: 95,622,586-95,655,642 GPR150, SPATA9, 2 more genes
    nsv4369969copy number variation1nstd173human GRCh37 chr5: 94,958,302-94,991,346 , GRCh38.p12 chr5: 95,622,598-95,655,642 SPATA9, GPR150, 2 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
    nsv4321173inversion1nstd166human GRCh37.p13 chr5: 86,365,040-130,339,409 , GRCh38.p12 chr5: 87,069,223-131,003,716 , APC, 481 more genes
    nsv3924896copy number variation1nstd102humanPathogenic GRCh38 chr5: 84,603,580-111,435,081 , GRCh37 chr5: 83,899,398-110,770,779 , NCBI36 chr5: 83,935,154-110,798,678 LOC107986438, GGCTP1, 254 more genes
    nsv3921454copy number variation1nstd102humanLikely benign GRCh38 chr5: 94,902,711-95,930,059 , NCBI36 chr5: 94,264,172-95,291,519 , GRCh37 chr5: 94,238,416-95,265,763 FAM81B, LOC102724720, 19 more genes
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