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Items: 1 to 20 of 116

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 more genes
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7073220inversion1nstd229human GRCh38 chr19: 45,719,988-49,018,157 , GRCh37.p13 chr19: 46,223,246-49,521,414 RUVBL2, NTN5, 150 more genes
    nsv7064020inversion1nstd229human GRCh38 chr19: 48,004,601-50,148,757 , GRCh37.p13 chr19: 48,507,858-50,652,014 TEAD2, LHB, 155 more genes
    nsv7017711copy number variation1nstd229human GRCh38 chr19: 48,387,101-48,401,300 , GRCh37.p13 chr19: 48,890,358-48,904,557 KDELR1, GRIN2D
    nsv7014397copy number variation1nstd229human GRCh38 chr19: 48,374,924-48,390,128 , GRCh37.p13 chr19: 48,878,181-48,893,385 SYNGR4, KDELR1
    nsv7012591copy number variation1nstd229human GRCh38 chr19: 48,384,368-48,386,739 , GRCh37.p13 chr19: 48,887,625-48,889,996 KDELR1
    nsv7012452copy number variation1nstd229human GRCh38 chr19: 45,998,776-48,954,957 , GRCh37.p13 chr19: 46,502,034-49,458,214 TMEM160, SNORD23, 131 more genes
    nsv6598038inversion1nstd223human GRCh38 chr19: 45,719,988-49,018,154 , GRCh37.p13 chr19: 46,223,246-49,521,411 PLEKHA4, GAPDHP38, 150 more genes
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6282070copy number variation1nstd214human GRCh38 chr19: 48,389,838-48,389,911 , GRCh37.p13 chr19: 48,893,095-48,893,168 , KDELR1
    nsv6216954copy number variation1nstd214human GRCh38 chr19: 48,390,172-48,390,282 , GRCh37.p13 chr19: 48,893,429-48,893,539 , KDELR1
    nsv6133704copy number variation1nstd213human GRCh37 chr19: 45,030,000-55,230,001 , GRCh38.p12 chr19: 44,525,967-54,071,460 AP2A1, APOC1, 582 more genes
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv6110571inversion1nstd212human GRCh38 chr19: 47,903,487-50,091,196 , GRCh37.p13 chr19: 48,406,744-50,594,453 , AP2A1, 155 more genes
    nsv6109305insertion1nstd212human GRCh38 chr19: 48,390,122-48,390,122 , GRCh37.p13 chr19: 48,893,379-48,893,379 , KDELR1
    nsv6054504copy number variation1nstd212human GRCh38 chr19: 48,386,238-48,386,734 , GRCh37.p13 chr19: 48,889,495-48,889,991 KDELR1
    nsv6043138copy number variation1nstd212human GRCh38 chr19: 48,389,879-48,389,951 , GRCh37.p13 chr19: 48,893,136-48,893,208 , KDELR1
    nsv5939182copy number variation1nstd209human GRCh38 chr19: 48,387,565-48,388,568 , GRCh37.p13 chr19: 48,890,822-48,891,825 KDELR1
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