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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970490inversion1nstd209human GRCh38 chr2: 240,811,836-241,011,847 , GRCh37.p13 chr2: 241,751,253-241,951,264 AGXT, KIF1A, 7 more genes
    nsv5952849insertion1nstd209human GRCh38 chr2: 240,869,074-240,869,074 , GRCh37.p13 chr2: 241,808,491-241,808,491 AGXT
    nsv5901336copy number variation1nstd209human GRCh38 chr2: 240,859,306-240,866,902 , GRCh37.p13 chr2: 241,798,723-241,806,319 AGXT
    nsv5901155copy number variation1nstd209human GRCh38 chr2: 240,879,898-240,879,953 , GRCh37.p13 chr2: 241,819,315-241,819,370 AGXT
    nsv5833131copy number variation1nstd209human GRCh38 chr2: 240,872,481-240,905,899 , GRCh37.p13 chr2: 241,811,898-241,845,316 CROCC2, AGXT, 1 more genes
    nsv5612694insertion1nstd207human GRCh38 chr2: 240,872,327-240,872,327 , GRCh37.p13 chr2: 241,811,744-241,811,744 AGXT
    nsv5609957insertion1nstd207human GRCh38 chr2: 240,869,074-240,869,074 , GRCh37.p13 chr2: 241,808,491-241,808,491 AGXT
    nsv5607699insertion1nstd207human GRCh38 chr2: 240,872,264-240,872,264 , GRCh37.p13 chr2: 241,811,681-241,811,681 AGXT
    nsv5448340copy number variation1nstd206human GRCh38 chr2: 240,879,030-240,881,744 , GRCh37.p13 chr2: 241,818,447-241,821,161 AGXT
    nsv5446389copy number variation1nstd206human GRCh38 chr2: 240,869,043-240,869,151 , GRCh37.p13 chr2: 241,808,460-241,808,568 AGXT
    nsv5387565copy number variation1nstd186human GRCh37 chr2: 241,811,589-241,811,905 , GRCh38.p12 chr2: 240,872,172-240,872,488 AGXT
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv4804741copy number variation1nstd200human GRCh37 chr2: 241,811,442-241,812,048 , GRCh38.p12 chr2: 240,872,025-240,872,631 AGXT
    nsv4790158copy number variation1nstd200human GRCh37 chr2: 241,798,723-241,806,320 , GRCh38.p12 chr2: 240,859,306-240,866,903 AGXT
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
    nsv4767308insertion1nstd199human GRCh37 chr2: 241,808,466-241,808,466 , GRCh38.p12 chr2: 240,869,049-240,869,049 AGXT
    nsv4759706insertion1nstd199human GRCh37 chr2: 241,811,598-241,811,598 , GRCh38.p12 chr2: 240,872,181-240,872,181 AGXT
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4726167insertion1nstd186human GRCh37 chr2: 241,808,460-241,808,460 , GRCh38.p12 chr2: 240,869,043-240,869,043 AGXT
    nsv4684239copy number variation1nstd102humanUncertain significance GRCh37 chr2: 238,863,455-243,048,760 , GRCh38.p12 chr2: 237,954,813-242,106,609 LOC285191, MTERF4, 103 more genes
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