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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5677721mobile element insertion1nstd211human GRCh38 chr7: 94,403,144-94,403,144 , GRCh37.p13 chr7: 94,032,456-94,032,456 COL1A2
    nsv5674023copy number variation1nstd102humanPathogenic GRCh37 chr7: 94,048,195-94,052,610 , GRCh38 chr7: 94,418,883-94,423,298 COL1A2
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5401568mobile element insertion1nstd206human GRCh38 chr7: 94,403,144-94,403,195 , GRCh37.p13 chr7: 94,032,456-94,032,507 COL1A2
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825168copy number variation1nstd200human GRCh37 chr7: 94,022,086-94,022,332 , GRCh38.p12 chr7: 94,392,774-94,393,020 COL1A2
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4729505copy number variation1nstd102humanUncertain significance GRCh37 chr7: 93,209,718-94,202,220 , GRCh38.p12 chr7: 93,580,406-94,572,908 LOC105375404, GNG11, 15 more genes
    nsv4728134copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 94,031,452-94,035,591 , GRCh38.p12 chr7: 94,402,140-94,406,279 COL1A2
    nsv4685981copy number variation1nstd102humanPathogenic GRCh37 chr7: 93,516,132-95,668,733 , GRCh38.p12 chr7: 93,886,820-96,039,421 LOC105375404, BET1, 36 more genes
    nsv4681353copy number variation1nstd102humanUncertain significance GRCh37 chr7: 94,024,334-94,214,837 , GRCh38.p12 chr7: 94,395,022-94,585,525 SGCE, LOC105375404, 3 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4451531copy number variation2nstd102humanPathogenic GRCh37 chr7: 94,037,139-94,038,155 , GRCh38 chr7: 94,407,827-94,408,843 COL1A2
    nsv4388620copy number variation1nstd171human GRCh37 chr7: 94,051,085-94,051,122 , GRCh38.p12 chr7: 94,421,773-94,421,810 COL1A2
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv3946732copy number variation1nstd167human GRCh37 chr7: 94,051,084-94,051,122 , GRCh38.p12 chr7: 94,421,772-94,421,810 COL1A2
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