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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5483905copy number variation1nstd206human GRCh38 chr9: 129,698,067-130,033,998 , GRCh37.p13 chr9: 132,460,346-132,796,277 MIR6855, PRRX2, 8 more genes
    nsv5250774copy number variation1nstd204human GRCh38.p13 chr9: 129,443,501-129,853,600 , GRCh37.p13 chr9: 132,205,780-132,615,879 ASB6, C9orf50, 12 more genes
    nsv5038901inversion1nstd200human GRCh38 chr9: 129,687,905-129,733,934 , GRCh37.p13 chr9: 132,450,184-132,496,213 PRRX2, PRRX2-AS1
    nsv4988470copy number variation1nstd200human GRCh38 chr9: 129,709,190-129,717,551 , GRCh37.p13 chr9: 132,471,469-132,479,830 PRRX2, PRRX2-AS1
    nsv4729432copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,470,092-133,044,256 , GRCh38.p12 chr9: 129,707,813-130,281,977 GPRACR, NCS1, 13 more genes
    nsv4729206copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,448,018-132,581,300 , GRCh38.p12 chr9: 129,685,739-129,819,021 PTGES, PRRX2-AS1, 4 more genes
    nsv4675061copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,449,936-132,795,093 , GRCh38.p12 chr9: 129,687,657-130,032,814 TOR1A, PRRX2, 8 more genes
    nsv4663874copy number variation1nstd186human GRCh37 chr9: 132,463,983-132,648,102 , GRCh38.p12 chr9: 129,701,704-129,885,823 C9orf78, PRRX2, 8 more genes
    nsv4653496copy number variation1nstd186human GRCh37 chr9: 132,463,983-132,648,102 , GRCh38.p12 chr9: 129,701,704-129,885,823 FNBP1, TOR1B, 8 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
    nsv4456688copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,183,626-133,431,092 , GRCh38.p12 chr9: 129,421,347-130,555,705 ASB6, GPR107, 22 more genes
    nsv4455331copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,449,921-132,793,004 , GRCh38.p12 chr9: 129,687,642-130,030,725 UBE2V1P4, MIR6855, 8 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
    nsv4367225copy number variation1nstd173human GRCh37 chr9: 132,449,937-132,582,750 , GRCh38.p12 chr9: 129,687,658-129,820,471 UBE2V1P4, PTGES, 4 more genes
    nsv4349353copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 131,670,024-134,514,071 , GRCh38.p12 chr9: 128,907,745-131,638,684 ABL1, ASS1, 69 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
    nsv4188943copy number variation1nstd166human GRCh37.p13 chr9: 132,381,207-132,732,472 , GRCh38.p12 chr9: 129,618,928-129,970,193 PRRX2-AS1, C9orf50, 11 more genes
    nsv4174387copy number variation1nstd166human GRCh37.p13 chr9: 132,472,521-132,474,545 , GRCh38.p12 chr9: 129,710,242-129,712,266 PRRX2, PRRX2-AS1
    nsv3924176copy number variation1nstd102humanUncertain significance NCBI36 chr9: 131,113,749-131,668,476 , GRCh37.p13 chr9: 132,073,928-132,628,655 , GRCh38.p12 chr9: 129,311,649-129,866,376 LOC105376292, PRRX2, 17 more genes
    nsv3923672copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,681,755-132,842,253 , GRCh38 chr9: 127,919,476-130,079,974 , NCBI36 chr9: 129,721,576-131,882,074 PIP5KL1, NTMT1, 80 more genes
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