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Items: 1 to 20 of 945

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137706insertion1nstd232human GRCh37.p13 chr2: 63,643,631-63,643,631 , GRCh38.p12 chr2: 63,416,496-63,416,496 WDPCP
    nsv7096899copy number variation1nstd102humanPathogenic GRCh37 chr2: 63,605,501-63,605,664 , GRCh38.p12 chr2: 63,378,366-63,378,529 WDPCP
    nsv7096898copy number variation1nstd102humanUncertain significance GRCh37 chr2: 63,540,363-63,667,025 , GRCh38.p12 chr2: 63,313,228-63,439,891 WDPCP
    nsv7096897copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 63,380,029-63,380,729 , GRCh38.p12 chr2: 63,152,894-63,153,594 WDPCP
    nsv7096674copy number variation1nstd102humanPathogenic GRCh37 chr2: 63,401,785-63,401,987 , GRCh38.p12 chr2: 63,174,650-63,174,852 WDPCP
    nsv7096673copy number variation1nstd102humanUncertain significance GRCh37 chr2: 63,380,029-63,401,987 , GRCh38.p12 chr2: 63,152,894-63,174,852 WDPCP
    nsv7096417copy number variation1nstd102humanPathogenic GRCh37 chr2: 63,815,311-63,815,405 , GRCh38.p12 chr2: 63,588,177-63,588,271 MDH1, WDPCP
    nsv7096416copy number variation1nstd102humanUncertain significance GRCh37 chr2: 63,660,859-63,667,025 , GRCh38.p12 chr2: 63,433,725-63,439,891 WDPCP
    nsv7096415copy number variation1nstd102humanUncertain significance GRCh37 chr2: 63,486,422-63,609,249 , GRCh38.p12 chr2: 63,259,287-63,382,114 WDPCP
    nsv7055384inversion1nstd229human GRCh38 chr2: 63,579,629-63,579,653 , GRCh37.p13 chr2: 63,806,763-63,806,787 WDPCP
    nsv7052112inversion1nstd229human GRCh38 chr2: 63,416,685-64,065,192 , GRCh37.p13 chr2: 63,643,820-64,292,326 RPL27P6, MDH1, 7 more genes
    nsv7047826inversion1nstd229human GRCh38 chr2: 63,423,041-63,884,116 , GRCh37.p13 chr2: 63,650,176-64,111,250 RPS4XP5, CSP1, 6 more genes
    nsv7047389inversion1nstd229human GRCh38 chr2: 63,230,857-63,450,259 , GRCh37.p13 chr2: 63,457,992-63,677,393 WDPCP, MTFR2P1
    nsv7045294inversion1nstd229human GRCh38 chr2: 63,528,131-63,535,961 , GRCh37.p13 chr2: 63,755,265-63,763,095 WDPCP
    nsv7042570inversion1nstd229human GRCh38 chr2: 63,318,884-63,322,095 , GRCh37.p13 chr2: 63,546,019-63,549,230 WDPCP
    nsv7041952inversion1nstd229human GRCh38 chr2: 63,526,866-63,555,739 , GRCh37.p13 chr2: 63,754,000-63,782,873 WDPCP
    nsv6676650copy number variation1nstd229human GRCh38 chr2: 63,200,901-63,281,900 , GRCh37.p13 chr2: 63,428,036-63,509,035 MTFR2P1, WDPCP, 1 more genes
    nsv6676495copy number variation1nstd229human GRCh38 chr2: 63,196,846-63,219,728 , GRCh37.p13 chr2: 63,423,981-63,446,863 WDPCP, LOC107985769
    nsv6676275copy number variation1nstd229human GRCh38 chr2: 63,203,501-63,220,200 , GRCh37.p13 chr2: 63,430,636-63,447,335 WDPCP
    nsv6675972copy number variation1nstd229human GRCh38 chr2: 63,204,776-63,204,964 , GRCh37.p13 chr2: 63,431,911-63,432,099 WDPCP
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