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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074516inversion1nstd229human GRCh38 chr19: 53,325,989-54,093,651 , GRCh37.p13 chr19: 53,829,242-54,528,887 MIR525, CACNG8, 93 more genes
    nsv7069393inversion1nstd229human GRCh38 chr19: 53,026,789-54,633,410 , GRCh37.p13 chr19: 53,530,042-54,528,887 MIR512-2, LILRB3, 145 more genes
    nsv7065131inversion1nstd229human GRCh38 chr19: 52,267,822-54,176,069 , GRCh37.p13 chr19: 52,771,075-54,528,887 ERVV-1, NDUFA3, 149 more genes
    nsv7064925inversion1nstd229human GRCh38 chr19: 49,540,460-54,108,860 , GRCh37.p13 chr19: 50,043,717-54,528,887 DPRX, EMC10, 323 more genes
    nsv7060687inversion1nstd229human GRCh38 chr19: 53,785,748-54,383,705 , GRCh37.p13 chr19|NW_004166865.1: 1-358,072 MBOAT7, VSTM1, 36 more genes
    nsv7058092inversion1nstd229human GRCh38 chr19: 53,519,606-54,093,763 , GRCh37.p13 chr19: 54,022,860-54,528,887 MIR512-2, MIR519A1, 78 more genes
    nsv6624795copy number variation1nstd224human GRCh37 chr19: 54,584,651-54,611,131 , GRCh38.p12 chr19: 54,081,382-54,107,824 , GRCh38.p12 chr19|NT_187693.1: 55,764-82,244 , GRCh38.p12 chr19|NW_003571061.2: 55,764-82,244 , GRCh38.p12 chr19|NW_003571057.2: 55,764-82,244 , GRCh38.p12 chr19|NW_003571058.2: 55,764-82,244 , GRCh38.p12 chr19|NW_003571059.2: 55,764-82,244 , GRCh38.p12 chr19|NW_003571060.1: 55,764-82,244 , GRCh38.p12 chr19|NW_003571056.2: 55,764-82,244 , GRCh38.p12 chr19|NW_003571055.2: 55,764-82,244 , GRCh38.p12 chr19|NW_003571054.1: 55,764-82,244 TFPT, OSCAR, 2 more genes
    nsv6599844inversion1nstd223human GRCh38 chr19: 54,093,238-54,093,340 , GRCh37.p13 chr19|NW_004166865.1: 67,605-67,707 OSCAR
    nsv6599207inversion1nstd223human GRCh38 chr19: 53,839,120-54,950,754 , GRCh37.p13 chr19|NW_004166865.1: 1-925,122 FCAR, KIR2DL1, 64 more genes
    nsv6597416inversion1nstd223human GRCh38 chr19: 53,217,793-54,175,150 , GRCh37.p13 chr19: 53,721,046-54,528,887 CACNG7, MIR371B, 110 more genes
    nsv6530259copy number variation1nstd223human GRCh38 chr19: 54,076,630-54,265,819 , GRCh37.p13 chr19|NW_004166865.1: 50,997-240,186 LOC107985279, RNU6-1307P, 16 more genes
    nsv6310493copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,297,303-55,678,016 , GRCh38.p12 chr19|NT_187693.1: 134,805-894,467 , GRCh38.p12 chr19: 53,794,049-55,166,648 PRPF31, TSEN34, 80 more genes
    nsv6278234copy number variation1nstd214human GRCh38 chr19: 54,096,487-54,096,595 , GRCh37.p13 chr19|NW_004166865.1: 70,854-70,962 OSCAR
    nsv6224517copy number variation1nstd214human GRCh38 chr19: 54,101,312-54,101,411 , GRCh37.p13 chr19|NW_004166865.1: 75,679-75,778 OSCAR, NDUFA3
    nsv6217343copy number variation1nstd214human GRCh38 chr19: 54,096,337-54,096,416 , GRCh37.p13 chr19|NW_004166865.1: 70,704-70,783 OSCAR
    nsv6106780insertion1nstd212human GRCh38 chr19: 54,095,594-54,095,594 , GRCh37.p13 chr19|NW_004166865.1: 69,961-69,961 OSCAR
    nsv6103582insertion1nstd212human GRCh38 chr19: 54,096,385-54,096,385 , GRCh37.p13 chr19|NW_004166865.1: 70,752-70,752 OSCAR
    nsv6058286copy number variation1nstd212human GRCh38 chr19: 54,101,741-54,101,799 , GRCh37.p13 chr19|NW_004166865.1: 76,108-76,166 OSCAR, NDUFA3
    nsv6049584copy number variation1nstd212human GRCh38 chr19: 54,099,175-54,099,272 , GRCh37.p13 chr19|NW_004166865.1: 73,542-73,639 OSCAR
    nsv6049116copy number variation1nstd212human GRCh38 chr19: 54,101,318-54,101,417 , GRCh37.p13 chr19|NW_004166865.1: 75,685-75,784 NDUFA3, OSCAR
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