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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095014copy number variation1nstd102humanUncertain significance GRCh37 chr18: 47,101,719-47,463,787 , GRCh38.p12 chr18: 49,575,349-49,937,417 SMUG1P1, SNHG22, 6 more genes
    nsv7074210inversion1nstd229human GRCh38 chr18: 45,861,287-52,164,943 , GRCh37.p13 chr18: 43,441,252-49,691,313 LOC105372100, RNA5SP458, 103 more genes
    nsv7064950inversion1nstd229human GRCh38 chr18: 49,426,149-50,066,271 , GRCh37.p13 chr18: 46,952,519-47,592,641 SRP72P1, C18orf32, 19 more genes
    nsv7062073inversion1nstd229human GRCh38 chr18: 42,140,183-50,368,023 , GRCh37.p13 chr18: 39,720,147-47,894,393 ACAA2, MIR4320, 105 more genes
    nsv7058348inversion1nstd229human GRCh38 chr18: 49,550,777-51,013,398 , GRCh37.p13 chr18: 47,077,147-48,539,768 SMUG1P1, CXXC1, 26 more genes
    nsv7017222copy number variation1nstd229human GRCh38 chr18: 49,821,084-49,822,631 , GRCh37.p13 chr18: 47,347,454-47,349,001 MYO5B, SNHG22
    nsv7015620copy number variation1nstd229human GRCh38 chr18: 48,566,814-53,963,212 , GRCh37.p13 chr18: 46,093,185-51,489,582 LINC02837, RPL29P32, 65 more genes
    nsv7011074copy number variation1nstd229human GRCh38 chr18: 49,835,008-49,837,675 , GRCh37.p13 chr18: 47,361,378-47,364,045 MYO5B, SNHG22
    nsv7009227copy number variation1nstd229human GRCh38 chr18: 49,809,959-49,816,281 , GRCh37.p13 chr18: 47,336,329-47,342,651 SCARNA17, SNHG22, 1 more genes
    nsv7005008copy number variation1nstd229human GRCh38 chr18: 49,818,629-49,818,760 , GRCh37.p13 chr18: 47,344,999-47,345,130 SNHG22
    nsv6998936copy number variation1nstd229human GRCh38 chr18: 49,574,421-49,939,057 , GRCh37.p13 chr18: 47,100,791-47,465,427 LIPG, LOC105372112, 6 more genes
    nsv6998934copy number variation1nstd229human GRCh38 chr18: 49,739,863-50,250,295 , GRCh37.p13 chr18: 47,266,233-47,776,665 RNA5SP457, MYO5B, 7 more genes
    nsv6998773copy number variation1nstd229human GRCh38 chr18: 44,716,377-50,773,277 , GRCh37.p13 chr18: 42,296,342-48,299,647 LOC105372101, MTCO2P2, 95 more genes
    nsv6595020inversion1nstd223human GRCh38 chr18: 49,148,101-52,144,680 , GRCh37.p13 chr18: 46,674,471-49,671,050 MYO5B, LIPG, 49 more genes
    nsv6530909copy number variation1nstd223human GRCh38 chr18: 49,574,421-49,939,057 , GRCh37.p13 chr18: 47,100,791-47,465,427 SNHG22, LOC105372112, 6 more genes
    nsv6518022copy number variation1nstd223human GRCh38 chr18: 49,812,901-49,815,000 , GRCh37.p13 chr18: 47,339,271-47,341,370 SNHG22, SCARNA17, 1 more genes
    nsv6516257copy number variation1nstd223human GRCh38 chr18: 49,791,101-49,817,700 , GRCh37.p13 chr18: 47,317,471-47,344,070 SCARNA17, ACAA2, 1 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6310262copy number variation1nstd102humanUncertain significance GRCh37 chr18: 46,570,425-48,604,837 , GRCh38.p12 chr18: 49,044,055-51,078,467 SNORD58C, SKA1, 40 more genes
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