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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5853190copy number variation1nstd209human GRCh38 chr9: 114,594,928-114,596,898 , GRCh37.p13 chr9: 117,357,208-117,359,178 ATP6V1G1
    nsv5248724copy number variation1nstd204human GRCh38.p13 chr9: 114,590,744-114,596,373 , GRCh37.p13 chr9: 117,353,024-117,358,653 ATP6V1G1
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983302copy number variation1nstd200human GRCh38 chr9: 114,596,276-114,598,686 , GRCh37.p13 chr9: 117,358,556-117,360,966 ATP6V1G1
    nsv4974844copy number variation1nstd200human GRCh38 chr9: 114,479,165-114,633,424 , GRCh37.p13 chr9: 117,241,445-117,395,704 , WHRN, 4 more genes
    nsv4974841copy number variation1nstd200human GRCh38 chr9: 114,188,704-114,694,720 , GRCh37.p13 chr9: 116,950,984-117,457,000 , TEX53, 14 more genes
    nsv4839127copy number variation1nstd200human GRCh37 chr9: 117,241,445-117,395,704 , GRCh38.p12 chr9: 114,479,165-114,633,424 , WHRN, 4 more genes
    nsv4836897copy number variation1nstd200human GRCh37 chr9: 117,358,556-117,360,966 , GRCh38.p12 chr9: 114,596,276-114,598,686 ATP6V1G1
    nsv4832438copy number variation1nstd200human GRCh37 chr9: 117,357,202-117,359,451 , GRCh38.p12 chr9: 114,594,922-114,597,171 ATP6V1G1
    nsv4729019copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,324,844-117,443,628 , GRCh38.p12 chr9: 114,562,564-114,681,348 TEX48, LOC107987121, 4 more genes
    nsv4675840copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,642,144-117,613,527 , GRCh38.p12 chr9: 113,879,864-114,851,247 COL27A1, LOC107987120, 20 more genes
    nsv4675463copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,270,143-117,497,954 , GRCh38.p12 chr9: 114,507,863-114,735,674 LOC105376229, ATP6V1G1, 5 more genes
    nsv4603206copy number variation1nstd183human GRCh37 chr9: 116,949,722-117,457,170 , GRCh38.p12 chr9: 114,187,442-114,694,890 , AKNA, 14 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456465copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,936,770-117,450,535 , GRCh38.p12 chr9: 114,174,490-114,688,255 WHRN, LOC100131877, 12 more genes
    nsv4456379copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,982,711-117,443,628 , GRCh38.p12 chr9: 111,220,431-114,681,348 MIR4668, LOC100418705, 74 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
    nsv4425372copy number variation1nstd174human GRCh37 chr9: 116,945,025-117,460,150 , GRCh38.p12 chr9: 114,182,745-114,697,870 , ORM1, 14 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4191991copy number variation1nstd166human GRCh37.p13 chr9: 117,341,489-117,357,283 , GRCh38.p12 chr9: 114,579,209-114,595,003 ATP6V1G1
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