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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147272copy number variation1nstd232human GRCh37.p13 chr22: 36,912,654-36,912,750 , GRCh38.p12 chr22: 36,516,607-36,516,703 EIF3D
    nsv7147033insertion1nstd232human GRCh37.p13 chr22: 36,920,035-36,920,035 , GRCh38.p12 chr22: 36,523,988-36,523,988 EIF3D
    nsv7146428insertion1nstd232human GRCh37.p13 chr22: 36,916,732-36,916,732 , GRCh38.p12 chr22: 36,520,685-36,520,685 EIF3D
    nsv7143041insertion1nstd232human GRCh37.p13 chr22: 36,920,782-36,920,782 , GRCh38.p12 chr22: 36,524,735-36,524,735 EIF3D
    nsv7142480insertion1nstd232human GRCh37.p13 chr22: 36,912,838-36,912,838 , GRCh38.p12 chr22: 36,516,791-36,516,791 EIF3D
    nsv7141258insertion1nstd232human GRCh37.p13 chr22: 36,920,034-36,920,034 , GRCh38.p12 chr22: 36,523,987-36,523,987 EIF3D
    nsv7138791insertion1nstd232human GRCh37.p13 chr22: 36,914,959-36,914,959 , GRCh38.p12 chr22: 36,518,912-36,518,912 EIF3D
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7072766inversion1nstd229human GRCh38 chr22: 35,603,617-39,341,195 , GRCh37.p13 chr22: 35,999,664-39,737,200 APOL5, MTATP6P20, 132 more genes
    nsv7072171inversion1nstd229human GRCh38 chr22: 34,919,966-36,817,658 , GRCh37.p13 chr22: 35,315,956-37,213,702 APOL4, RBFOX2, 45 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7064066inversion1nstd229human GRCh38 chr22: 34,920,312-39,418,308 , GRCh37.p13 chr22: 35,316,302-39,814,313 LOC112268295, APOBEC3B-AS1, 150 more genes
    nsv7061356inversion1nstd229human GRCh38 chr22: 36,105,612-36,614,159 , GRCh37.p13 chr22: 36,501,660-37,010,206 MTATP6P20, CACNG2, 18 more genes
    nsv7059210inversion1nstd229human GRCh38 chr22: 35,603,611-39,337,136 , GRCh37.p13 chr22: 35,999,658-39,733,141 MTCO2P20, RPS29P31, 132 more genes
    nsv7034493copy number variation1nstd229human GRCh38 chr22: 36,298,457-36,572,532 , GRCh37.p13 chr22: 36,694,503-36,968,579 MYH9, CACNG2, 7 more genes
    nsv7028199copy number variation1nstd229human GRCh38 chr22: 36,502,101-36,508,921 , GRCh37.p13 chr22: 36,898,148-36,904,968 EIF3D, FOXRED2
    nsv7025871copy number variation1nstd229human GRCh38 chr22: 36,514,064-36,514,089 , GRCh37.p13 chr22: 36,910,111-36,910,136 EIF3D
    nsv7024654copy number variation1nstd229human GRCh38 chr22: 36,352,908-37,059,696 , GRCh37.p13 chr22: 36,748,953-37,455,736 NCF4-AS1, TST, 23 more genes
    nsv6637947copy number variation1nstd102humanUncertain significance GRCh37 chr22: 36,751,242-36,971,521 , GRCh38.p12 chr22: 36,355,197-36,575,474 RPS15AP38, CACNG2, 7 more genes
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