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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv7054180inversion1nstd229human GRCh38 chr1: 89,266,025-89,266,106 , GRCh37.p13 chr1: 89,731,708-89,731,789 GBP5, LOC100421401
    nsv7052082inversion1nstd229human GRCh38 chr1: 89,196,206-89,404,308 , GRCh37.p13 chr1: 89,661,889-89,869,867 GBP4, CAPNS1P1, 5 more genes
    nsv7051476inversion1nstd229human GRCh38 chr1: 87,647,529-89,769,769 , GRCh37.p13 chr1: 88,113,212-90,235,328 RBMXL1, PTGES3P1, 35 more genes
    nsv7045277inversion1nstd229human GRCh38 chr1: 89,219,136-91,269,986 , GRCh37.p13 chr1: 89,684,819-91,735,543 LOC105378847, CAPNS1P1, 33 more genes
    nsv7042360inversion1nstd229human GRCh38 chr1: 89,189,894-89,972,465 , GRCh37.p13 chr1: 89,655,577-90,438,024 LRRC8B, LRRC8C-DT, 16 more genes
    nsv7038668inversion1nstd229human GRCh38 chr1: 88,971,917-89,507,849 , GRCh37.p13 chr1: 89,437,600-89,973,408 LOC107985076, LOC105378842, 17 more genes
    nsv6656992copy number variation1nstd229human GRCh38 chr1: 89,250,791-89,261,406 , GRCh37.p13 chr1: 89,716,474-89,727,089 LOC100421401, GBP5
    nsv6656764copy number variation1nstd229human GRCh38 chr1: 89,271,742-89,273,965 , GRCh37.p13 chr1: 89,737,425-89,739,648 LOC100421401, GBP5
    nsv6656537copy number variation1nstd229human GRCh38 chr1: 89,238,756-89,384,832 , GRCh37.p13 chr1: 89,704,439-89,850,391 GBP5, GBP6, 2 more genes
    nsv6655953copy number variation1nstd229human GRCh38 chr1: 88,934,901-89,331,900 , GRCh37.p13 chr1: 89,400,584-89,797,583 PTGES3P1, GBP4, 13 more genes
    nsv6626480copy number variation1nstd224human GRCh37 chr1: 89,587,610-90,005,132 , GRCh38.p12 chr1: 89,121,927-89,539,573 GBP5, LOC100421401, 12 more genes
    nsv6542421inversion1nstd223human GRCh38 chr1: 85,951,963-92,104,665 , GRCh37.p13 chr1: 86,417,646-92,570,222 LOC105378844, LINC01773, 104 more genes
    nsv6327592copy number variation1nstd223human GRCh38 chr1: 89,271,742-89,273,965 , GRCh37.p13 chr1: 89,737,425-89,739,648 LOC100421401, GBP5
    nsv6313574copy number variation1nstd102humanPathogenic GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400 RNA5SP51, ADGRL4, 315 more genes
    nsv6296321copy number variation1nstd186human GRCh37 chr1: 89,716,474-89,727,089 , GRCh38.p12 chr1: 89,250,791-89,261,406 LOC100421401, GBP5
    nsv6167440copy number variation1nstd214human GRCh38 chr1: 89,273,153-89,273,230 , GRCh37.p13 chr1: 89,738,836-89,738,913 GBP5, LOC100421401
    nsv6134255copy number variation1nstd213human GRCh37 chr1: 89,570,000-90,560,001 , GRCh38.p12 chr1: 89,104,317-90,094,443 GBP5, GBP1P1, 24 more genes
    nsv5887480copy number variation1nstd209human GRCh38 chr1: 89,273,153-89,273,230 , GRCh37.p13 chr1: 89,738,836-89,738,913 LOC100421401, GBP5
    nsv5729506mobile element insertion1nstd211human GRCh38 chr1: 89,267,901-89,267,901 , GRCh37.p13 chr1: 89,733,584-89,733,584 GBP5, LOC100421401
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