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Items: 1 to 20 of 160

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148237copy number variation1nstd102humanUncertain significance GRCh38 chr19: 47,257,435-47,886,413 , GRCh37.p13 chr19: 47,760,692-48,389,670 KPTN, RPL23AP80, 22 more genes
    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
    nsv7076581inversion1nstd229human GRCh38 chr19: 47,308,308-47,317,705 , GRCh37.p13 chr19: 47,811,565-47,820,962 C5AR1
    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
    nsv7072237inversion1nstd229human GRCh38 chr19: 47,047,927-47,435,103 , GRCh37.p13 chr19: 47,551,185-47,938,360 MIR3190, C5AR1, 11 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
    nsv7017498copy number variation1nstd229human GRCh38 chr19: 47,317,240-47,322,539 , GRCh37.p13 chr19: 47,820,497-47,825,796 C5AR1
    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
    nsv6596034inversion1nstd223human GRCh38 chr19: 47,316,148-47,317,193 , GRCh37.p13 chr19: 47,819,405-47,820,450 C5AR1
    nsv6531366copy number variation1nstd223human GRCh38 chr19: 47,314,556-47,316,598 , GRCh37.p13 chr19: 47,817,813-47,819,855 C5AR1
    nsv6530892copy number variation1nstd223human GRCh38 chr19: 47,298,749-47,308,602 , GRCh37.p13 chr19: 47,802,006-47,811,859 C5AR1
    nsv6522205copy number variation1nstd223human GRCh38 chr19: 47,322,023-47,323,077 , GRCh37.p13 chr19: 47,825,280-47,826,334 C5AR1
    nsv6521580copy number variation1nstd223human GRCh38 chr19: 47,318,326-47,342,377 , GRCh37.p13 chr19: 47,821,583-47,845,634 C5AR2, C5AR1
    nsv6515885copy number variation1nstd223human GRCh38 chr19: 47,304,386-47,316,571 , GRCh37.p13 chr19: 47,807,643-47,819,828 C5AR1
    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
    nsv5553603insertion1nstd206human GRCh38 chr19: 47,316,619-47,316,655 , GRCh37.p13 chr19: 47,819,876-47,819,912 C5AR1
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