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Items: 1 to 20 of 347

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057047inversion1nstd229human GRCh38 chr4: 107,704,515-107,759,133 , GRCh37.p13 chr4: 108,625,671-108,680,289 PAPSS1
    nsv7050540inversion1nstd229human GRCh38 chr4: 107,658,938-107,658,982 , GRCh37.p13 chr4: 108,580,094-108,580,138 PAPSS1
    nsv7048471inversion1nstd229human GRCh38 chr4: 107,711,068-107,712,798 , GRCh37.p13 chr4: 108,632,224-108,633,954 PAPSS1
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv7042286inversion1nstd229human GRCh38 chr4: 107,196,729-108,480,148 , GRCh37.p13 chr4: 108,117,886-109,401,304 RAC1P5, ZACNP1, 15 more genes
    nsv6751959copy number variation1nstd229human GRCh38 chr4: 107,701,978-107,775,028 , GRCh37.p13 chr4: 108,623,134-108,696,184 PAPSS1
    nsv6751500copy number variation1nstd229human GRCh38 chr4: 107,619,754-107,622,682 , GRCh37.p13 chr4: 108,540,910-108,543,838 PAPSS1
    nsv6749849copy number variation1nstd229human GRCh38 chr4: 103,966,147-109,668,724 , GRCh37.p13 chr4: 104,887,304-110,589,880 CYP2U1-AS1, OSTC, 66 more genes
    nsv6748664copy number variation1nstd229human GRCh38 chr4: 107,702,843-107,709,528 , GRCh37.p13 chr4: 108,623,999-108,630,684 PAPSS1
    nsv6748550copy number variation1nstd229human GRCh38 chr4: 107,705,694-107,706,022 , GRCh37.p13 chr4: 108,626,850-108,627,178 PAPSS1
    nsv6745591copy number variation1nstd229human GRCh38 chr4: 107,688,753-107,692,603 , GRCh37.p13 chr4: 108,609,909-108,613,759 PAPSS1
    nsv6744221copy number variation1nstd229human GRCh38 chr4: 107,692,107-107,701,259 , GRCh37.p13 chr4: 108,613,263-108,622,415 PAPSS1
    nsv6629335copy number variation1nstd224human GRCh37 chr4: 108,493,334-108,603,171 , GRCh38.p12 chr4: 107,572,177-107,682,015 LOC105377358, PAPSS1
    nsv6629281copy number variation1nstd224human GRCh37 chr4: 108,639,491-108,732,508 , GRCh38.p12 chr4: 107,718,335-107,811,352 PAPSS1
    nsv6394248copy number variation1nstd223human GRCh38 chr4: 107,690,806-107,691,275 , GRCh37.p13 chr4: 108,611,962-108,612,431 PAPSS1
    nsv6390259copy number variation1nstd223human GRCh38 chr4: 107,619,754-107,622,682 , GRCh37.p13 chr4: 108,540,910-108,543,838 PAPSS1
    nsv6385615copy number variation1nstd223human GRCh38 chr4: 107,654,554-107,654,966 , GRCh37.p13 chr4: 108,575,710-108,576,122 PAPSS1
    nsv6385545copy number variation1nstd223human GRCh38 chr4: 107,683,460-107,683,900 , GRCh37.p13 chr4: 108,604,616-108,605,056 PAPSS1
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
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