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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098079copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,717,738-2,719,115 , GRCh38.p12 chr9: 2,717,738-2,719,115 KCNV2
    nsv7097968copy number variation1nstd102humanUncertain significance GRCh37 chr9: 676,973-2,729,727 , GRCh38.p12 chr9: 676,973-2,729,727 RN7SL592P, LOC102723803, 23 more genes
    nsv7097951copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,717,758-2,728,666 , GRCh38.p12 chr9: 2,717,758-2,728,666 KCNV2
    nsv7097950copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,717,755-2,728,666 , GRCh38.p12 chr9: 2,717,755-2,728,666 KCNV2
    nsv7097718copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,622,190-2,729,727 , GRCh38.p12 chr9: 2,622,190-2,729,727 VLDLR, KCNV2, 2 more genes
    nsv7093337copy number variation1nstd102humanPathogenic GRCh38 chr9: 2,718,842-2,718,929 , GRCh37 chr9: 2,718,842-2,718,929 KCNV2
    nsv7076573inversion1nstd229human GRCh38 chr9: 2,695,836-2,783,337 , GRCh37.p13 chr9: 2,695,836-2,783,337 KCNV2
    nsv7066230inversion1nstd229human GRCh38 chr9: 235,930-9,843,002 , GRCh37.p13 chr9: 235,930-9,843,002 GLIS3-AS1, LOC105375955, 118 more genes
    nsv7065614inversion1nstd229human GRCh38 chr9: 102,865-4,490,246 , GRCh37.p13 chr9: 102,865-4,490,246 RFX3, LOC102723803, 52 more genes
    nsv6878015copy number variation1nstd229human GRCh38 chr9: 2,667,664-2,750,045 , GRCh37.p13 chr9: 2,667,664-2,750,045 KCNV2, LOC105375957
    nsv6877807copy number variation1nstd229human GRCh38 chr9: 2,705,213-2,755,779 , GRCh37.p13 chr9: 2,705,213-2,755,779 KCNV2
    nsv6876291copy number variation1nstd229human GRCh38 chr9: 2,676,380-3,058,454 , GRCh37.p13 chr9: 2,676,380-3,058,454 ATP5PDP2, KCNV2, 3 more genes
    nsv6876083copy number variation1nstd229human GRCh38 chr9: 2,699,272-2,720,747 , GRCh37.p13 chr9: 2,699,272-2,720,747 KCNV2
    nsv6876020copy number variation1nstd229human GRCh38 chr9: 2,717,701-2,728,600 , GRCh37.p13 chr9: 2,717,701-2,728,600 KCNV2
    nsv6873424copy number variation1nstd229human GRCh38 chr9: 2,710,901-2,719,500 , GRCh37.p13 chr9: 2,710,901-2,719,500 KCNV2
    nsv6873221copy number variation1nstd229human GRCh38 chr9: 2,721,565-2,743,906 , GRCh37.p13 chr9: 2,721,565-2,743,906 KCNV2
    nsv6872142copy number variation1nstd229human GRCh38 chr9: 2,677,425-2,729,876 , GRCh37.p13 chr9: 2,677,425-2,729,876 KCNV2
    nsv6871604copy number variation1nstd229human GRCh38 chr9: 2,701,795-2,733,643 , GRCh37.p13 chr9: 2,701,795-2,733,643 KCNV2
    nsv6870717copy number variation1nstd229human GRCh38 chr9: 2,725,274-2,801,543 , GRCh37.p13 chr9: 2,725,274-2,801,543 KCNV2
    nsv6869599copy number variation1nstd229human GRCh38 chr9: 2,718,172-2,729,912 , GRCh37.p13 chr9: 2,718,172-2,729,912 KCNV2
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