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Items: 1 to 20 of 99

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5024694copy number variation1nstd200human GRCh38 chr19: 43,578,119-43,578,468 , GRCh37.p13 chr19: 44,082,271-44,082,620 PINLYP
    nsv5024672copy number variation1nstd200human GRCh38 chr19: 42,797,406-43,578,600 , GRCh37.p13 chr19: 43,301,558-44,082,752 , PINLYP, 28 more genes
    nsv4679272copy number variation1nstd189human GRCh37.p13 chr19: 43,906,705-44,198,705 , GRCh38.p12 chr19: 43,402,553-43,694,553 , PLAUR, 16 more genes
    nsv4457468copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,818,072-44,100,076 , GRCh38.p12 chr19: 43,313,920-43,595,924 CD177, LYPD3, 11 more genes
    nsv4457412copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,803,157-44,105,375 , GRCh38.p12 chr19: 43,299,005-43,601,223 ZNF575, CEACAMP4, 12 more genes
    nsv4457378copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,004,424-44,080,746 , GRCh38.p12 chr19: 43,500,272-43,576,594 ETHE1, PHLDB3, 3 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv3920763copy number variation1nstd102humanUncertain significance NCBI36 chr19: 48,534,223-49,049,155 , GRCh38 chr19: 43,338,231-43,853,163 , GRCh37 chr19: 43,842,383-44,357,315 SRRM5, RN7SL368P, 23 more genes
    nsv3919276copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,807,486-44,080,610 , GRCh38 chr19: 43,303,334-43,576,458 , NCBI36 chr19: 48,499,326-48,772,450 PRG1, LOC110467528, 10 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3891669copy number variation1nstd102humanPathogenic GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277 MIR320E, BCL3, 189 more genes
    nsv3880735copy number variation1nstd102humanLikely pathogenic GRCh38 chr19: 41,608,672-44,315,856 , GRCh37.p13 chr19: 42,514,712-44,820,009 ATP1A3, CEACAM1, 114 more genes
    nsv3168446copy number variation1nstd158human GRCh37 chr19: 35,445,908-45,506,757 , GRCh38.p12 chr19: 34,955,004-45,003,499 , ACTN4, 449 more genes
    nsv3165583copy number variation1nstd151human GRCh37 chr19: 43,857,865-44,097,524 , GRCh38.p12 chr19: 43,353,713-43,593,372 ETHE1, PHLDB3, 9 more genes
    nsv2757532copy number variation1nstd130human GRCh37 chr19: 266,034-54,723,310 , GRCh38.p12 chr19: 266,034-54,071,460 , BABAM1, 2197 more genes
    nsv2752158copy number variation1nstd130human GRCh37 chr19: 289,244-58,996,454 , GRCh38.p12 chr19: 289,244-58,485,087 , NFKBIB, 2456 more genes
    nsv1961710short tandem repeat1nstd128human GRCh37 chr19: 44,083,401-44,083,415 , GRCh38.p12 chr19: 43,579,249-43,579,263 PINLYP
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