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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096704copy number variation1nstd102humanUncertain significance GRCh37 chr3: 168,802,697-172,835,521 , GRCh38.p12 chr3: 169,084,909-173,117,731 GHSR, KLF7P1, 67 more genes
    nsv7048483inversion1nstd229human GRCh38 chr3: 169,821,268-170,002,421 , GRCh37.p13 chr3: 169,539,056-169,720,209 SAMD7, FHL1P1, 5 more genes
    nsv7047264inversion1nstd229human GRCh38 chr3: 168,346,425-172,414,638 , GRCh37.p13 chr3: 168,064,213-172,132,428 RNU4-38P, LINC01997, 60 more genes
    nsv7044294inversion1nstd229human GRCh38 chr3: 169,921,498-169,921,949 , GRCh37.p13 chr3: 169,639,286-169,639,737 SAMD7
    nsv7041278inversion1nstd229human GRCh38 chr3: 169,919,839-169,921,803 , GRCh37.p13 chr3: 169,637,627-169,639,591 SAMD7
    nsv6734704copy number variation1nstd229human GRCh38 chr3: 169,926,759-169,939,925 , GRCh37.p13 chr3: 169,644,547-169,657,713 FAM20BP1, SAMD7
    nsv6734370copy number variation1nstd229human GRCh38 chr3: 169,917,057-169,920,004 , GRCh37.p13 chr3: 169,634,845-169,637,792 SAMD7
    nsv6731687copy number variation1nstd229human GRCh38 chr3: 169,773,099-169,962,497 , GRCh37.p13 chr3: 169,490,887-169,680,285 MYNN, LRRC34, 6 more genes
    nsv6730741copy number variation1nstd229human GRCh38 chr3: 169,895,217-169,919,690 , GRCh37.p13 chr3: 169,613,005-169,637,478 SAMD7, KRT18P43
    nsv6726436copy number variation1nstd229human GRCh38 chr3: 169,934,290-169,939,680 , GRCh37.p13 chr3: 169,652,078-169,657,468 SAMD7
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6636764copy number variation1nstd102humanUncertain significance GRCh37 chr3: 168,718,767-169,662,001 , GRCh38.p12 chr3: 169,000,979-169,944,213 LRRIQ4, MECOM, 17 more genes
    nsv6569261inversion1nstd223human GRCh38 chr3: 169,918,243-169,918,856 , GRCh37.p13 chr3: 169,636,031-169,636,644 SAMD7
    nsv6568350inversion1nstd223human GRCh38 chr3: 169,918,084-169,918,987 , GRCh37.p13 chr3: 169,635,872-169,636,775 SAMD7
    nsv6555884inversion1nstd223human GRCh38 chr3: 169,821,268-170,002,422 , GRCh37.p13 chr3: 169,539,056-169,720,210 SEC62, LRRC31, 5 more genes
    nsv6366357copy number variation1nstd223human GRCh38 chr3: 169,923,610-169,924,356 , GRCh37.p13 chr3: 169,641,398-169,642,144 SAMD7
    nsv6311968copy number variation1nstd102humanUncertain significance GRCh37 chr3: 169,482,388-170,130,102 , GRCh38.p12 chr3: 169,764,600-170,412,314 TRV-AAC1-1, SEC62, 19 more genes
    nsv6298338copy number variation1nstd186human GRCh37 chr3: 169,627,989-169,628,155 , GRCh38.p12 chr3: 169,910,201-169,910,367 SAMD7
    nsv6297003copy number variation1nstd186human GRCh37 chr3: 169,581,299-169,636,431 , GRCh38.p12 chr3: 169,863,511-169,918,643 LRRC31, KRT18P43, 1 more genes
    nsv6291110copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 168,118,411-179,867,071 , GRCh38.p12 chr3: 168,400,623-180,149,283 ACTL6A, ECT2, 141 more genes
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