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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137151copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 47,028,919-48,185,409 , GRCh38.p12 chr19: 46,525,662-47,682,152 C5AR1, CALM3, 36 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
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    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
    nsv7012120copy number variation1nstd229human GRCh38 chr19: 46,631,756-46,635,159 , GRCh37.p13 chr19: 47,135,013-47,138,416 GNG8
    nsv7011248copy number variation1nstd229human GRCh38 chr19: 46,631,282-46,643,499 , GRCh37.p13 chr19: 47,134,539-47,146,756 GNG8
    nsv6598038inversion1nstd223human GRCh38 chr19: 45,719,988-49,018,154 , GRCh37.p13 chr19: 46,223,246-49,521,411 PLEKHA4, GAPDHP38, 150 more genes
    nsv6515727copy number variation1nstd223human GRCh38 chr19: 46,628,261-46,632,088 , GRCh37.p13 chr19: 47,131,518-47,135,345 GNG8
    nsv6310639copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,104,692-47,260,195 , GRCh38.p12 chr19: 46,601,435-46,756,938 PTGIR, PRKD2, 10 more genes
    nsv6210242copy number variation1nstd214human GRCh38 chr19: 46,635,608-46,635,760 , GRCh37.p13 chr19: 47,138,865-47,139,017 GNG8
    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
    nsv6111978insertion1nstd212human GRCh38 chr19: 46,635,537-46,635,537 , GRCh37.p13 chr19: 47,138,794-47,138,794 GNG8
    nsv6105912insertion1nstd212human GRCh38 chr19: 46,635,674-46,635,674 , GRCh37.p13 chr19: 47,138,931-47,138,931 GNG8
    nsv6041337copy number variation1nstd212human GRCh38 chr19: 46,635,555-46,635,623 , GRCh37.p13 chr19: 47,138,812-47,138,880 GNG8
    nsv5649170insertion1nstd207human GRCh38 chr19: 46,635,646-46,635,646 , GRCh37.p13 chr19: 47,138,903-47,138,903 GNG8
    nsv5602714copy number variation1nstd207human GRCh38 chr19: 46,635,556-46,635,740 , GRCh37.p13 chr19: 47,138,813-47,138,997 GNG8
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