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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7049289inversion1nstd229human GRCh38 chr4: 1,879,237-2,966,412 , GRCh37.p13 chr4: 1,880,964-2,968,139 RNF4, SCARNA22, 28 more genes
    nsv7039441inversion1nstd229human GRCh38 chr4: 1,689,472-2,959,448 , GRCh37.p13 chr4: 1,691,199-2,961,175 NOP14-AS1, LOC112268460, 34 more genes
    nsv6737787copy number variation1nstd229human GRCh38 chr4: 1,968,064-1,970,889 , GRCh37.p13 chr4: 1,969,791-1,972,616 NSD2
    nsv6736417copy number variation1nstd229human GRCh38 chr4: 1,801,401-1,870,600 , GRCh37.p13 chr4: 1,803,128-1,872,327 RN7SL671P, LETM1, 2 more genes
    nsv6728071copy number variation1nstd229human GRCh38 chr4: 1,874,444-1,880,456 , GRCh37.p13 chr4: 1,876,171-1,882,183 NSD2
    nsv6725253copy number variation1nstd229human GRCh38 chr4: 1,904,596-1,907,428 , GRCh37.p13 chr4: 1,906,323-1,909,155 NSD2
    nsv6722686copy number variation1nstd229human GRCh38 chr4: 1,890,923-1,893,582 , GRCh37.p13 chr4: 1,892,650-1,895,309 NSD2
    nsv6721814copy number variation1nstd229human GRCh38 chr4: 1,872,039-1,883,156 , GRCh37.p13 chr4: 1,873,766-1,884,883 NSD2
    nsv6721023copy number variation1nstd229human GRCh38 chr4: 1,886,069-1,891,038 , GRCh37.p13 chr4: 1,887,796-1,892,765 NSD2
    nsv6720374copy number variation1nstd229human GRCh38 chr4: 1,970,252-2,008,474 , GRCh37.p13 chr4: 1,971,979-2,010,201 MIR943, SCARNA22, 2 more genes
    nsv6718544copy number variation1nstd229human GRCh38 chr4: 1,874,401-1,880,500 , GRCh37.p13 chr4: 1,876,128-1,882,227 NSD2
    nsv6636691copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,346-2,437,290 , GRCh38.p12 chr4: 68,454-2,435,563 SPON2, TACC3, 77 more genes
    nsv6636600copy number variation1nstd102humanUncertain significance GRCh37 chr4: 1,892,740-2,503,033 , GRCh38.p12 chr4: 1,891,013-2,501,306 LOC105374352, POLN, 19 more genes
    nsv6636582copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359 NELFA, OR7E111FP, 289 more genes
    nsv6636548copy number variation1nstd102humanUncertain significance GRCh37 chr4: 1,734,046-1,871,531 , GRCh38.p12 chr4: 1,732,319-1,869,804 NSD2, TACC3, 4 more genes
    nsv6636534copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 963,688-2,913,553 , GRCh38.p12 chr4: 969,900-2,911,826 ADD1, CTBP1, 53 more genes
    nsv6636435copy number variation1nstd102humanUncertain significance GRCh37 chr4: 1,904,862-2,009,467 , GRCh38.p12 chr4: 1,903,135-2,007,740 MIR943, SCARNA22, 2 more genes
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