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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5294229copy number variation1nstd204human GRCh38.p13 chr19: 1,717,401-2,347,800 , GRCh37.p13 chr19: 1,717,400-2,347,798 DOT1L, LOC107985278, 32 more genes
    nsv5291342copy number variation1nstd204human GRCh38.p13 chr19: 879,901-2,550,600 , GRCh37.p13 chr19: 879,901-2,550,598 LOC105372240, ELOCP28, 92 more genes
    nsv5014306copy number variation1nstd200human GRCh38 chr19: 2,229,923-2,295,815 , GRCh37.p13 chr19: 2,229,922-2,295,814 MIR4321, MIR6789, 10 more genes
    nsv4676366copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 1,075,192-2,256,387 , GRCh38.p12 chr19: 1,075,193-2,256,388 AMH, ATP5F1D, 64 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 AZU1, REEP6, 159 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4627750copy number variation1nstd183human GRCh37 chr19: 2,250,661-2,250,810 , GRCh38.p12 chr19: 2,250,662-2,250,811 JSRP1, AMH, 1 more genes
    nsv4621272copy number variation1nstd183human GRCh37 chr19: 2,145,005-2,466,296 , GRCh38.p12 chr19: 2,145,006-2,466,298 LMNB2, LINC01775, 19 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4452268copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,406,030-3,597,207 , GRCh38.p12 chr19: 1,406,031-3,597,209 C19orf25, MIR7108, 92 more genes
    nsv4436611copy number variation1nstd102humanUncertain significance GRCh37 chr19: 2,229,488-4,004,142 , GRCh38.p12 chr19: 2,229,489-4,004,144 LMNB2, SF3A2, 76 more genes
    nsv4265888copy number variation1nstd166human GRCh37.p13 chr19: 2,237,453-2,274,873 , GRCh38.p12 chr19: 2,237,454-2,274,874 AMH, OAZ1, 5 more genes
    nsv4262549copy number variation1nstd166human GRCh37.p13 chr19: 2,223,363-2,275,618 , GRCh38.p12 chr19: 2,223,364-2,275,619 PLEKHJ1, MIR1227, 9 more genes
    nsv4256971copy number variation1nstd166human GRCh37.p13 chr19: 2,198,578-2,338,093 , GRCh38.p12 chr19: 2,198,579-2,338,094 AMH, DOT1L, 13 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 POLR2E, PWWP3A, 283 more genes
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 DAPK3, IZUMO4, 214 more genes
    nsv3921932copy number variation1nstd102humanPathogenic NCBI36 chr19: 210,395-2,506,147 , GRCh37 chr19: 259,395-2,555,147 , GRCh38 chr19: 259,395-2,555,149 GZMM, MIER2, 129 more genes
    nsv3920078copy number variation1nstd102humanUncertain significance GRCh38 chr19: 1,351,163-2,555,149 , NCBI36 chr19: 1,302,162-2,506,147 , GRCh37 chr19: 1,351,162-2,555,147 MKNK2, LOC101928543, 61 more genes
    nsv3915373copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,516,574-4,059,126 , GRCh37 chr19: 1,565,574-4,108,126 , GRCh38 chr19: 1,565,575-4,108,128 LOC100419704, DIRAS1, 104 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 more genes
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