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Items: 1 to 20 of 38

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv544537copy number variation2nstd54human NCBI36 chr22: 17,299,469-17,404,821 , GRCh37.p13 chr22: 18,919,469-19,024,821 , GRCh38.p12 chr22: 18,931,956-19,037,308 PRODH, DGCR5, 2 more genes
    nsv544535copy number variation1nstd54human NCBI36 chr22: 17,041,723-19,835,418 , GRCh37.p13 chr22: 18,661,723-21,505,418 , GRCh38.p12 chr22: 18,178,956-21,151,129 , RN7SKP131, 133 more genes
    nsv544534copy number variation1nstd54human NCBI36 chr22: 17,021,230-17,404,821 , GRCh37.p13 chr22: 18,641,230-19,024,821 , GRCh38.p12 chr22: 18,158,463-19,037,308 , FAM230J, 31 more genes
    nsv544532copy number variation1nstd54human NCBI36 chr22: 17,015,796-19,770,515 , GRCh37.p13 chr22: 18,635,796-21,440,515 , GRCh38.p12 chr22: 18,153,029-21,086,226 , LOC100129262, 130 more genes
    nsv544531copy number variation2nstd54human NCBI36 chr22: 17,008,018-20,269,974 , GRCh37.p13 chr22: 18,628,018-21,939,974 , GRCh38.p12 chr22: 18,145,251-21,585,685 , P2RX6, 154 more genes
    nsv544530copy number variation15nstd54human NCBI36 chr22: 17,008,018-19,770,515 , GRCh37.p13 chr22: 18,628,018-21,440,515 , GRCh38.p12 chr22: 18,145,251-21,086,226 , FAM230G, 130 more genes
    nsv544528copy number variation1nstd54human NCBI36 chr22: 17,007,819-19,737,831 , GRCh37.p13 chr22: 18,627,819-21,407,831 , GRCh38.p12 chr22: 18,145,052-21,053,542 , LOC107985584, 128 more genes
    nsv544527copy number variation1nstd54human NCBI36 chr22: 17,007,818-20,270,122 , GRCh37.p13 chr22: 18,627,818-21,940,122 , GRCh38.p12 chr22: 18,145,051-21,585,833 , TUBA3GP, 154 more genes
    nsv544509copy number variation4nstd54human NCBI36 chr22: 15,908,677-18,626,906 , GRCh37.p13 chr22: 17,528,677-20,246,906 , GRCh38.p12 chr22: 17,047,787-20,259,383 , RTL10, 121 more genes
    nsv544506copy number variation1nstd54human NCBI36 chr22: 15,464,954-18,659,821 , GRCh37.p13 chr22: 17,084,954-20,279,821 , GRCh38.p12 chr22: 16,604,064-20,292,298 , TANGO2, 141 more genes
    nsv518950copy number variation1nstd21human NCBI35 chr22: 18,681,547-19,290,109 , GRCh37.p13 chr22: 20,306,993-20,965,555 , GRCh38.p12 chr22: 18,339,130-20,611,268 , ARVCF, 100 more genes
    nsv516997copy number variation54nstd21human NCBI35 chr22: 17,001,191-17,401,167 , GRCh37.p13 chr22: 18,626,637-19,026,613 , GRCh38.p12 chr22: 18,143,870-19,039,100 , LOC105372858, 31 more genes
    nsv491547copy number variation2nstd45humanPathogenic GRCh38.p12 chr22: 18,924,718-20,299,685 , GRCh37 chr22: 18,912,231-20,287,208 ARVCF, COMT, 60 more genes
    nsv491538copy number variation2nstd45humanPathogenic GRCh38.p12 chr22: 18,339,130-21,111,383 , GRCh37 chr22: 18,912,231-21,465,672 ARVCF, COMT, 127 more genes
    esv34520copy number variation3estd55human NCBI35 chr22: 17,014,854-17,411,293 , GRCh37.p13 chr22: 18,640,300-19,036,739 , GRCh38.p12 chr22: 18,157,533-19,049,226 , GGT3P, 32 more genes
    esv34431copy number variation3estd55human NCBI35 chr22: 17,265,521-17,410,786 , GRCh37.p13 chr22: 18,890,967-19,036,232 , GRCh38.p12 chr22: 18,903,454-19,048,719 PRODH, DGCR6, 4 more genes
    nsv482354copy number variation1nstd40human NCBI34 chr22: 17,308,436-17,440,893 , GRCh38.p12 chr22: 18,946,369-19,078,826 , GRCh37.p13 chr22: 18,933,882-19,066,339 DGCR2, DGCR11, 3 more genes
    nsv482225copy number variation1nstd40human GRCh37 chr22: 17,900,001-25,900,000 , GRCh38.p12 chr22: 17,420,954-25,504,033 , ADORA2A, 398 more genes
    nsv482224copy number variation1nstd40human GRCh38.p12 chr22: 17,420,954-25,504,033 , GRCh37 chr22: 17,900,001-25,900,000 , ADORA2A, 398 more genes
    nsv459397copy number variation1nstd27human NCBI35 chr22: 17,287,232-19,786,907 , GRCh37.p13 chr22: 18,912,678-21,462,353 , GRCh38.p12 chr22: 18,339,130-21,108,064 , ARVCF, 126 more genes
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