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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5538520insertion1nstd206human GRCh38 chr16: 75,627,169-75,627,220 , GRCh37.p13 chr16: 75,661,067-75,661,118 KARS1
    nsv5146831mobile element insertion1nstd203human GRCh38 chr16: 75,640,792-75,640,811 , GRCh37.p13 chr16: 75,674,690-75,674,709 KARS1
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005874copy number variation1nstd200human GRCh38 chr16: 75,630,765-75,703,758 , GRCh37.p13 chr16: 75,664,663-75,737,656 TERF2IP, KARS1, 3 more genes
    nsv5005873copy number variation1nstd200human GRCh38 chr16: 75,619,210-75,640,630 , GRCh37.p13 chr16: 75,653,108-75,674,528 ADAT1, KARS1
    nsv5005871copy number variation1nstd200human GRCh38 chr16: 75,551,267-75,905,440 , GRCh37.p13 chr16: 75,585,165-75,939,338 LOC105371347, KARS1, 11 more genes
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4857745copy number variation1nstd200human GRCh37 chr16: 75,679,719-75,679,793 , GRCh38.p12 chr16: 75,645,821-75,645,895 TERF2IP, KARS1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729987copy number variation1nstd102humanUncertain significance GRCh37 chr16: 75,554,118-75,823,234 , GRCh38.p12 chr16: 75,520,220-75,789,336 LOC105371348, CPHXL2, 10 more genes
    nsv4729944copy number variation1nstd102humanUncertain significance GRCh37 chr16: 75,281,963-75,665,698 , GRCh38.p12 chr16: 75,248,065-75,631,800 KARS1, TMEM170A, 10 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4622615copy number variation1nstd183human GRCh37 chr16: 75,588,506-75,855,475 , GRCh38.p12 chr16: 75,554,608-75,821,577 TERF2IP, ATP5PBP7, 9 more genes
    nsv4618895copy number variation1nstd183human GRCh37 chr16: 75,681,443-75,681,598 , GRCh38.p12 chr16: 75,647,545-75,647,700 KARS1, TERF2IP
    nsv4551057insertion1nstd166human GRCh37.p13 chr16: 75,661,053-75,661,053 , GRCh38.p12 chr16: 75,627,155-75,627,155 KARS1
    nsv4457330copy number variation1nstd102humanUncertain significance GRCh37 chr16: 72,677,179-77,439,111 , GRCh38.p12 chr16: 72,643,280-77,405,214 MON1B, PSMD7, 70 more genes
    nsv4456930copy number variation1nstd102humanUncertain significance GRCh37 chr16: 75,275,780-75,684,031 , GRCh38.p12 chr16: 75,241,882-75,650,133 RNU6-758P, ADAT1, 11 more genes
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4321328inversion1nstd166human GRCh37.p13 chr16: 67,701,568-75,754,137 , GRCh38.p12 chr16: 67,667,665-75,720,239 , CDH3, 203 more genes
    nsv4252007copy number variation1nstd166human GRCh37.p13 chr16: 75,676,785-75,676,865 , GRCh38.p12 chr16: 75,642,887-75,642,967 KARS1
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