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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970828inversion1nstd209human GRCh38 chr9: 104,706,998-105,087,317 , GRCh37.p13 chr9: 107,469,279-107,849,598 ABCA1, NIPSNAP3A, 5 more genes
    nsv5490505copy number variation1nstd206human GRCh38 chr9: 104,759,903-104,765,468 , GRCh37.p13 chr9: 107,522,184-107,527,749 NIPSNAP3B, NIPSNAP3A
    nsv5490442copy number variation1nstd206human GRCh38 chr9: 104,765,095-104,765,187 , GRCh37.p13 chr9: 107,527,376-107,527,468 NIPSNAP3B
    nsv5484282copy number variation1nstd206human GRCh38 chr9: 104,761,699-104,776,683 , GRCh37.p13 chr9: 107,523,980-107,538,964 NIPSNAP3B
    nsv5484153copy number variation1nstd206human GRCh38 chr9: 104,767,945-104,773,106 , GRCh37.p13 chr9: 107,530,226-107,535,387 NIPSNAP3B
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4982964copy number variation1nstd200human GRCh38 chr9: 104,765,629-104,767,380 , GRCh37.p13 chr9: 107,527,910-107,529,661 NIPSNAP3B
    nsv4982963copy number variation1nstd200human GRCh38 chr9: 104,759,903-104,765,468 , GRCh37.p13 chr9: 107,522,184-107,527,749 NIPSNAP3B, NIPSNAP3A
    nsv4837662copy number variation1nstd200human GRCh37 chr9: 107,522,184-107,527,749 , GRCh38.p12 chr9: 104,759,903-104,765,468 NIPSNAP3A, NIPSNAP3B
    nsv4835294copy number variation1nstd200human GRCh37 chr9: 107,530,226-107,535,387 , GRCh38.p12 chr9: 104,767,945-104,773,106 NIPSNAP3B
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4679196copy number variation1nstd189human GRCh37.p13 chr9: 107,061,882-107,737,966 , GRCh38.p12 chr9: 104,299,601-104,975,685 ABCA1, NIPSNAP3A, 18 more genes
    nsv4614276copy number variation1nstd183human GRCh37 chr9: 107,530,171-107,535,336 , GRCh38.p12 chr9: 104,767,890-104,773,055 NIPSNAP3B
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455409copy number variation1nstd102humanUncertain significance GRCh37 chr9: 106,618,735-107,897,515 , GRCh38.p12 chr9: 103,856,454-105,135,234 LOC107987105, OR13D1, 27 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4413690copy number variation1nstd174human GRCh37 chr9: 107,530,153-107,535,392 , GRCh38.p12 chr9: 104,767,872-104,773,111 NIPSNAP3B
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4177994copy number variation1nstd166human GRCh37.p13 chr9: 107,527,915-107,529,657 , GRCh38.p12 chr9: 104,765,634-104,767,376 NIPSNAP3B
    nsv4175723copy number variation1nstd166human GRCh37.p13 chr9: 107,522,184-107,527,749 , GRCh38.p12 chr9: 104,759,903-104,765,468 NIPSNAP3B, NIPSNAP3A
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