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Items: 1 to 20 of 112

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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
    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
    nsv7062448inversion1nstd229human GRCh38 chr19: 47,486,012-47,487,980 , GRCh37.p13 chr19: 47,989,269-47,991,237 NAPA-AS1, NAPA, 1 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
    nsv6598038inversion1nstd223human GRCh38 chr19: 45,719,988-49,018,154 , GRCh37.p13 chr19: 46,223,246-49,521,411 PLEKHA4, GAPDHP38, 150 more genes
    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
    nsv5529144copy number variation1nstd206human GRCh38 chr19: 47,479,551-47,479,608 , GRCh37.p13 chr19: 47,982,808-47,982,865 KPTN
    nsv5293275copy number variation1nstd204human GRCh38.p13 chr19: 47,049,201-47,476,100 , GRCh37.p13 chr19: 47,552,459-47,979,357 , ZC3H4, 12 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4676350copy number variation1nstd102humanUncertain significance GRCh37 chr19: 45,531,056-48,174,177 , GRCh38.p12 chr19: 45,027,798-47,670,920 NKPD1, IGFL1, 112 more genes
    nsv4676254copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,331,662-48,234,260 , GRCh38.p12 chr19: 46,828,405-47,731,003 AP2S1, BICRA, 22 more genes
    nsv4626594copy number variation1nstd183human GRCh37 chr19: 47,986,617-47,986,774 , GRCh38.p12 chr19: 47,483,360-47,483,517 NAPA-AS1, KPTN
    nsv4624453copy number variation1nstd183human GRCh37 chr19: 47,834,906-47,977,877 , GRCh38.p12 chr19: 47,331,649-47,474,620 C5AR2, SLC8A2, 3 more genes
    nsv4457518copy number variation1nstd102humanUncertain significance GRCh37 chr19: 47,785,567-48,178,258 , GRCh38.p12 chr19: 47,282,310-47,675,001 C5AR2, DHX34, 9 more genes
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