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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    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
    nsv5113333mobile element insertion1nstd203human GRCh38 chr7: 93,972,118-93,972,133 , GRCh37.p13 chr7: 93,601,430-93,601,445 , BET1
    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
    nsv4957705copy number variation1nstd200human GRCh38 chr7: 93,984,393-93,985,041 , GRCh37.p13 chr7: 93,613,705-93,614,353 , BET1
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    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
    nsv4729398copy number variation1nstd102humanUncertain significance GRCh37 chr7: 93,588,920-93,783,393 , GRCh38.p12 chr7: 93,959,608-94,154,081 BET1, BET1-AS1
    nsv4715619copy number variation1nstd195human GRCh37 chr7: 93,422,601-93,787,501 , GRCh38.p12 chr7: 93,793,289-94,158,189 , GNG11, 7 more genes
    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
    nsv4567851sequence alteration1nstd166human GRCh37.p13 chr7: 93,612,815-93,612,816 , GRCh38.p12 chr7: 93,983,503-93,983,504 , BET1
    nsv4485719mobile element insertion1nstd166human GRCh37.p13 chr7: 93,610,275-93,610,275 , GRCh38.p12 chr7: 93,980,963-93,980,963 , BET1
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4384112copy number variation1nstd173human GRCh37 chr7: 93,440,986-93,607,295 , GRCh38.p12 chr7: 93,811,674-93,977,983 , GNG11, 6 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3916221copy number variation1nstd102humanPathogenic NCBI36 chr7: 92,754,488-94,797,369 , GRCh37.p13 chr7: 92,916,552-94,959,433 , GRCh38.p12 chr7: 93,287,240-95,330,121 BET1-AS1, RN7SKP129, 33 more genes
    nsv3914094copy number variation1nstd102humanPathogenic GRCh38 chr7: 84,002,634-95,228,883 , GRCh37 chr7: 83,631,950-94,858,195 , NCBI36 chr7: 83,469,886-94,696,131 LINC03017, MIR1285-1, 121 more genes
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