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Items: 1 to 20 of 1797

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124592insertion1nstd186human GRCh37 chr3: 192,376,517-192,376,517 , GRCh38.p12 chr3: 192,658,728-192,658,728 FGF12
    nsv5964739insertion1nstd209human GRCh38 chr3: 192,691,815-192,691,815 , GRCh37.p13 chr3: 192,409,604-192,409,604 FGF12
    nsv5959577insertion1nstd209human GRCh38 chr3: 192,167,754-192,167,754 , GRCh37.p13 chr3: 191,885,543-191,885,543 FGF12
    nsv5958950insertion1nstd209human GRCh38 chr3: 192,327,576-192,327,576 , GRCh37.p13 chr3: 192,045,365-192,045,365 FGF12
    nsv5957883insertion1nstd209human GRCh38 chr3: 192,537,950-192,537,950 , GRCh37.p13 chr3: 192,255,739-192,255,739 FGF12
    nsv5956187insertion1nstd209human GRCh38 chr3: 192,664,602-192,664,602 , GRCh37.p13 chr3: 192,382,391-192,382,391 , FGF12
    nsv5950838insertion1nstd209human GRCh38 chr3: 192,669,602-192,669,602 , GRCh37.p13 chr3: 192,387,391-192,387,391 , FGF12
    nsv5949116insertion1nstd209human GRCh38 chr3: 192,658,728-192,658,728 , GRCh37.p13 chr3: 192,376,517-192,376,517 FGF12
    nsv5907250copy number variation1nstd209human GRCh38 chr3: 192,219,542-192,270,856 , GRCh37.p13 chr3: 191,937,331-191,988,645 FGF12-AS1, FGF12
    nsv5907165copy number variation1nstd209human GRCh38 chr3: 192,546,872-192,550,501 , GRCh37.p13 chr3: 192,264,661-192,268,290 FGF12
    nsv5905625copy number variation1nstd209human GRCh38 chr3: 192,172,160-192,173,522 , GRCh37.p13 chr3: 191,889,949-191,891,311 FGF12
    nsv5902327copy number variation1nstd209human GRCh38 chr3: 192,688,157-192,886,819 , GRCh37.p13 chr3: 192,405,946-192,604,608 RNU1-20P, LOC107986056, 2 more genes
    nsv5901944copy number variation1nstd209human GRCh38 chr3: 192,711,263-192,711,389 , GRCh37.p13 chr3: 192,429,052-192,429,178 FGF12
    nsv5901452copy number variation1nstd209human GRCh38 chr3: 192,587,087-192,595,024 , GRCh37.p13 chr3: 192,304,876-192,312,813 FGF12
    nsv5901149copy number variation1nstd209human GRCh38 chr3: 192,345,392-192,345,701 , GRCh37.p13 chr3: 192,063,181-192,063,490 FGF12
    nsv5899778copy number variation1nstd209human GRCh38 chr3: 192,138,296-192,138,633 , GRCh37.p13 chr3: 191,856,085-191,856,422 FGF12
    nsv5899602copy number variation1nstd209human GRCh38 chr3: 192,179,436-192,180,166 , GRCh37.p13 chr3: 191,897,225-191,897,955 FGF12
    nsv5898529copy number variation1nstd209human GRCh38 chr3: 192,715,490-192,715,647 , GRCh37.p13 chr3: 192,433,279-192,433,436 FGF12
    nsv5891480copy number variation1nstd209human GRCh38 chr3: 192,404,979-192,405,667 , GRCh37.p13 chr3: 192,122,768-192,123,456 FGF12
    nsv5890773copy number variation1nstd209human GRCh38 chr3: 192,377,958-192,378,482 , GRCh37.p13 chr3: 192,095,747-192,096,271 FGF12
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