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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
    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
    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
    nsv6555884inversion1nstd223human GRCh38 chr3: 169,821,268-170,002,422 , GRCh37.p13 chr3: 169,539,056-169,720,210 SEC62, LRRC31, 5 more genes
    nsv6367543copy number variation1nstd223human GRCh38 chr3: 169,955,035-169,956,674 , GRCh37.p13 chr3: 169,672,823-169,674,462 FHL1P1
    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
    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
    nsv6061106insertion1nstd212human GRCh38 chr3: 169,962,273-169,962,273 , GRCh37.p13 chr3: 169,680,061-169,680,061 FHL1P1
    nsv5685660mobile element insertion1nstd211human GRCh38 chr3: 169,960,403-169,960,403 , GRCh37.p13 chr3: 169,678,191-169,678,191 FHL1P1
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5397861mobile element insertion1nstd206human GRCh38 chr3: 169,960,403-169,960,454 , GRCh37.p13 chr3: 169,678,191-169,678,242 FHL1P1
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4920647copy number variation1nstd200human GRCh38 chr3: 169,965,626-169,965,730 , GRCh37.p13 chr3: 169,683,414-169,683,518 FHL1P1, SEC62
    nsv4920646copy number variation1nstd200human GRCh38 chr3: 169,955,035-169,956,674 , GRCh37.p13 chr3: 169,672,823-169,674,462 FHL1P1
    nsv4798516copy number variation1nstd200human GRCh37 chr3: 169,683,414-169,683,518 , GRCh38.p12 chr3: 169,965,626-169,965,730 FHL1P1, SEC62
    nsv4798515copy number variation1nstd200human GRCh37 chr3: 169,672,823-169,674,463 , GRCh38.p12 chr3: 169,955,035-169,956,675 FHL1P1
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
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