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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057594inversion1nstd229human GRCh38 chr7: 66,159,073-66,513,347 , GRCh37.p13 chr7: 65,624,060-65,978,334 GTF2IP9, LINC00174, 8 more genes
    nsv7050458inversion1nstd229human GRCh38 chr7: 66,139,390-67,448,632 , GRCh37.p13 chr7: 65,604,377-66,913,619 SAPCD2P3, SPDYE21, 32 more genes
    nsv7041397inversion1nstd229human GRCh38 chr7: 65,600,026-71,276,703 , GRCh37.p13 chr7: 65,286,678-70,741,689 GALNT17, MTCO1P25, 74 more genes
    nsv6836176copy number variation1nstd229human GRCh38 chr7: 66,182,225-66,462,992 , GRCh37.p13 chr7: 65,647,212-65,927,979 LOC729126, GTF2IP9, 4 more genes
    nsv6835608copy number variation1nstd229human GRCh38 chr7: 65,825,345-66,840,559 , GRCh37.p13 chr7: 65,290,332-66,305,546 LOC346329, RABGEF1P1, 27 more genes
    nsv6831775copy number variation1nstd229human GRCh38 chr7: 66,372,516-66,761,743 , GRCh37.p13 chr7: 65,837,503-66,226,730 SAPCD2P3, RABGEF1, 13 more genes
    nsv6825632copy number variation1nstd229human GRCh38 chr7: 66,418,335-66,426,856 , GRCh37.p13 chr7: 65,883,322-65,891,843 SKP1P1
    nsv6822638copy number variation1nstd229human GRCh38 chr7: 66,423,130-66,620,537 , GRCh37.p13 chr7: 65,888,117-66,085,524 LOC107986704, SKP1P1, 7 more genes
    nsv6820566copy number variation1nstd229human GRCh38 chr7: 66,065,907-66,553,205 , GRCh37.p13 chr7: 65,530,894-66,018,192 LINC00174, RABGEF1P1, 12 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6619322copy number variation1nstd223human GRCh38 chr7: 66,418,320-66,426,855 , GRCh37.p13 chr7: 65,883,307-65,891,842 SKP1P1
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6312786copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 65,556,983-66,460,414 , GRCh38.p12 chr7: 66,091,996-66,995,427 ASL, SKP1P1, 27 more genes
    nsv6291136copy number variation1nstd102humanUncertain significance GRCh37 chr7: 64,651,626-66,010,636 , GRCh38.p12 chr7: 65,191,248-66,545,649 SNORA22, LOC105375334, 35 more genes
    nsv6135778copy number variation1nstd213human GRCh37 chr7: 65,440,000-66,120,001 , GRCh38.p12 chr7: 65,975,013-66,655,014 ASL, CRCP, 20 more genes
    nsv6135777copy number variation1nstd213human GRCh37 chr7: 65,150,000-70,530,001 , GRCh38.p12 chr7: 65,685,031-71,065,015 ASL, GUSB, 72 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5322525inversion1nstd204human GRCh37.p13 chr7: 65,776,458-71,393,640 , GRCh38.p13 chr7: 66,311,471-71,928,655 , SKP1P1, 64 more genes
    nsv5117071mobile element insertion1nstd203human GRCh38 chr7: 66,421,657-66,421,672 , GRCh37.p13 chr7: 65,886,644-65,886,659 SKP1P1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
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