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Items: 1 to 20 of 215

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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
    nsv7148162copy number variation1nstd102humanUncertain significance GRCh38 chr19: 47,794,370-47,886,413 , GRCh37.p13 chr19: 48,297,627-48,389,670 SULT2A1, RPL23AP80, 4 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
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7016187copy number variation1nstd229human GRCh38 chr19: 47,873,050-47,877,811 , GRCh37.p13 chr19: 48,376,307-48,381,068 SULT2A1
    nsv7015638copy number variation1nstd229human GRCh38 chr19: 47,857,624-47,872,961 , GRCh37.p13 chr19: 48,360,881-48,376,218 TPRX2, SULT2A1, 1 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
    nsv7010390copy number variation1nstd229human GRCh38 chr19: 47,869,861-47,870,405 , GRCh37.p13 chr19: 48,373,118-48,373,662 LINC01595, SULT2A1
    nsv7008555copy number variation1nstd229human GRCh38 chr19: 47,869,901-47,871,100 , GRCh37.p13 chr19: 48,373,158-48,374,357 SULT2A1
    nsv7006703copy number variation1nstd229human GRCh38 chr19: 47,872,868-47,876,242 , GRCh37.p13 chr19: 48,376,125-48,379,499 SULT2A1
    nsv7006602copy number variation1nstd229human GRCh38 chr19: 47,876,169-47,890,236 , GRCh37.p13 chr19: 48,379,426-48,393,493 SULT2A1
    nsv7001510copy number variation1nstd229human GRCh38 chr19: 47,884,201-47,887,200 , GRCh37.p13 chr19: 48,387,458-48,390,457 SULT2A1
    nsv7001100copy number variation1nstd229human GRCh38 chr19: 47,798,750-47,883,072 , GRCh37.p13 chr19: 48,302,007-48,386,329 SULT2A1, CRX, 3 more genes
    nsv7000979copy number variation1nstd229human GRCh38 chr19: 47,861,856-47,876,016 , GRCh37.p13 chr19: 48,365,113-48,379,273 SULT2A1, LINC01595, 1 more genes
    nsv6625218copy number variation1nstd224human GRCh37 chr19: 48,381,128-48,401,893 , GRCh38.p12 chr19: 47,877,871-47,898,636 SULT2A1
    nsv6625029copy number variation1nstd224human GRCh37 chr19: 48,323,733-48,406,374 , GRCh38.p12 chr19: 47,820,476-47,903,117 SULT2A1, TPRX2, 2 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
    nsv6597431inversion1nstd223human GRCh38 chr19: 47,872,762-47,875,163 , GRCh37.p13 chr19: 48,376,019-48,378,420 SULT2A1
    nsv6596373inversion1nstd223human GRCh38 chr19: 47,865,482-47,872,761 , GRCh37.p13 chr19: 48,368,739-48,376,018 LINC01595, SULT2A1
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