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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5696741mobile element insertion1nstd211human GRCh38 chr19: 41,448,236-41,448,236 , GRCh37.p13 chr19: 41,954,141-41,954,141 , GRCh37.p13 chr19|NW_004775434.1: 17,275-17,275 LOC107985329, DMAC2
    nsv5532611copy number variation1nstd206human GRCh38 chr19: 41,436,138-41,436,193 , GRCh37.p13 chr19|NW_004775434.1: 5,177-5,232 , GRCh37.p13 chr19: 41,942,043-41,942,098 DMAC2
    nsv5518392copy number variation1nstd206human GRCh38 chr19: 41,445,871-41,447,386 , GRCh37.p13 chr19|NW_004775434.1: 14,910-16,425 , GRCh37.p13 chr19: 41,951,776-41,953,291 LOC107985329, DMAC2
    nsv5375311translocation1nstd200human GRCh38 chr19: 11,183,172-11,183,172 , GRCh38 chr19: 41,445,991-41,445,991 , GRCh37.p13 chr19|NW_004775434.1: 15,030-15,030 , GRCh37.p13 chr19: 11,293,848-11,293,848 , GRCh37.p13 chr19: 41,951,896-41,951,896 DMAC2, KANK2
    nsv5288731copy number variation1nstd204human GRCh38.p13 chr19: 41,182,901-41,435,300 , GRCh37.p13 chr19: 41,688,806-41,936,866 LOC105372401, AXL, 13 more genes
    nsv5024653copy number variation1nstd200human GRCh38 chr19: 41,351,628-41,450,794 , GRCh37.p13 chr19: 41,857,533-41,936,866 BCKDHA, B9D2, 7 more genes
    nsv5020485copy number variation1nstd200human GRCh38 chr19: 41,445,367-41,447,716 , GRCh37.p13 chr19: 41,951,272-41,953,621 , GRCh37.p13 chr19|NW_004775434.1: 14,406-16,755 LOC107985329, DMAC2
    nsv5020484copy number variation1nstd200human GRCh38 chr19: 41,436,135-41,442,059 , GRCh37.p13 chr19: 41,942,040-41,947,964 , GRCh37.p13 chr19|NW_004775434.1: 5,174-11,098 DMAC2, ERICH4
    nsv4868415copy number variation1nstd200human GRCh37 chr19: 41,952,195-41,952,886 , GRCh38.p12 chr19: 41,446,290-41,446,981 LOC107985329, DMAC2
    nsv4865179copy number variation1nstd200human GRCh37 chr19: 41,857,533-41,956,699 , GRCh38.p12 chr19: 41,351,628-41,450,794 B9D2, BCKDHA, 7 more genes
    nsv4676231copy number variation1nstd102humanUncertain significance GRCh37 chr19: 41,889,319-42,338,832 , GRCh38.p12 chr19: 41,383,414-41,834,777 , GRCh38.p12 chr19|NT_187620.1: 1-233,762 CEACAM7, LYPD4, 25 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
    nsv4423584copy number variation1nstd174human GRCh37 chr19: 41,949,829-42,008,216 , GRCh38.p12 chr19: 41,443,924-41,502,300 , GRCh38.p12 chr19|NT_187620.1: 188,043-233,762 DMAC2, ERICH4, 2 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
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 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
    nsv3169031copy number variation1nstd158human GRCh38.p12 chr19: 38,412,977-41,901,266 , GRCh37 chr19: 38,903,617-42,405,416 , ACTN4, 162 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
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