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Items: 1 to 20 of 57

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673968copy number variation1nstd102humanPathogenic GRCh37 chr9: 80,851,267-80,858,572 , GRCh38.p12 chr9: 78,236,351-78,243,656 CEP78
    nsv7098101copy number variation1nstd102humanPathogenic GRCh37 chr9: 80,851,266-80,856,548 , GRCh38.p12 chr9: 78,236,350-78,241,632 CEP78
    nsv7098203copy number variation1nstd102humanPathogenic GRCh37 chr9: 80,854,919-80,856,735 , GRCh38.p12 chr9: 78,240,003-78,241,819 CEP78
    nsv6314275insertion1nstd102humanPathogenic GRCh37 chr9: 80,869,809-80,869,809 , GRCh38 chr9: 78,254,893-78,254,893 CEP78
    nsv4436066complex substitution1nstd102humanPathogenic GRCh38.p12 chr9: 78,228,782-78,244,763 , GRCh37 chr9: 80,843,698-80,859,679 CEP78
    nsv7148179copy number variation1nstd102humanLikely pathogenic GRCh38 chr9: 78,235,965-78,243,734 , GRCh37.p13 chr9: 80,850,881-80,858,650 CEP78
    nsv3908965copy number variation1nstd102humanLikely benign GRCh37 chr9: 80,850,226-80,880,439 , GRCh38.p12 chr9: 78,235,310-78,265,523 CEP78
    nsv6313111copy number variation1nstd102humanUncertain significance GRCh37 chr9: 80,881,497-80,888,713 , GRCh38.p12 chr9: 78,266,581-78,273,797 CEP78
    nsv7098474copy number variation1nstd102humanUncertain significance GRCh37 chr9: 80,881,338-80,881,678 , GRCh38.p12 chr9: 78,266,422-78,266,762 CEP78
    nsv6313291copy number variation1nstd102humanUncertain significance GRCh37 chr9: 80,861,565-80,863,809 , GRCh38.p12 chr9: 78,246,649-78,248,893 CEP78
    nsv3898724copy number variation1nstd102humanUncertain significance GRCh37 chr9: 80,833,575-80,973,771 , GRCh38.p12 chr9: 78,218,659-78,358,855 CEP78, LOC107987082, 2 more genes
    nsv3897053copy number variation1nstd102humanPathogenic GRCh37 chr9: 68,999,534-84,656,998 , GRCh38.p12 chr9: 40,926,305-82,042,083 CEP78, PABIR1, 397 more genes
    nsv3893036copy number variation1nstd102humanPathogenic GRCh37 chr9: 68,838,523-83,340,723 , GRCh38.p12 chr9: 40,915,719-80,725,808 CEP78, RPL35AP21, 379 more genes
    nsv3915174copy number variation1nstd102humanPathogenic NCBI36 chr9: 70,304,266-85,474,962 , GRCh38 chr9: 68,499,530-83,670,227 , GRCh37 chr9: 71,130,848-86,285,142 CEP78, LOC107987086, 183 more genes
    nsv4455928copy number variation1nstd102humanPathogenic GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877 CEP78, RPL35AP21, 134 more genes
    nsv3904790copy number variation1nstd102humanPathogenic GRCh37 chr9: 74,534,790-84,014,155 , GRCh38.p12 chr9: 71,919,874-81,399,240 CEP78, LOC105376099, 108 more genes
    nsv3913411copy number variation1nstd102humanPathogenic NCBI36 chr9: 75,511,422-82,175,364 , GRCh37 chr9: 76,321,602-82,985,544 , GRCh38 chr9: 73,706,686-80,370,629 CEP78, OTX2P1, 72 more genes
    nsv6312943copy number variation1nstd102humanPathogenic GRCh37 chr9: 79,792,621-80,944,002 , GRCh38.p12 chr9: 77,177,705-78,329,086 CEP78, RPL21P84, 14 more genes
    nsv3912247copy number variation1nstd102humanPathogenic NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981 CEP78, ALOX15P2, 2184 more genes
    nsv3890420copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797 CEP78, TBC1D13, 2183 more genes
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