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Items: 1 to 20 of 296

  • The following term was not found in dbVar: lgooxc.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv1851330copy number variation1estd188human NCBI36 chr7: 72,384,584-72,405,387 , GRCh37.p13 chr7|NW_003871064.1: 861,881-882,678 , GRCh37.p13 chr7: 72,746,648-72,767,451 , GRCh38.p12 chr7: 73,332,645-73,353,442 FKBP6, RNU6-1080P
    esv1849903copy number variation1estd188human NCBI36 chr7: 72,384,584-72,405,387 , GRCh37.p13 chr7|NW_003871064.1: 861,881-882,678 , GRCh37.p13 chr7: 72,746,648-72,767,451 , GRCh38.p12 chr7: 73,332,645-73,353,442 RNU6-1080P, FKBP6
    esv1849661copy number variation1estd188human NCBI36 chr7: 72,386,436-72,400,365 , GRCh37.p13 chr7|NW_003871064.1: 863,732-877,656 , GRCh37.p13 chr7: 72,748,500-72,762,429 , GRCh38.p12 chr7: 73,334,496-73,348,420 RNU6-1080P, FKBP6
    esv1848841copy number variation1estd188human NCBI36 chr7: 72,386,436-72,400,365 , GRCh37.p13 chr7|NW_003871064.1: 863,732-877,656 , GRCh37.p13 chr7: 72,748,500-72,762,429 , GRCh38.p12 chr7: 73,334,496-73,348,420 FKBP6, RNU6-1080P
    esv3771850copy number variation1estd192human GRCh37 chr7: 72,752,239-72,752,472 , GRCh38.p12 chr7: 73,338,236-73,338,469 RNU6-1080P, FKBP6
    esv1233459copy number variation1estd22human NCBI36 chr7: 72,389,269-72,389,270 , GRCh37.p13 chr7|NW_003871064.1: 866,566-866,567 , GRCh37.p13 chr7: 72,751,333-72,751,334 , GRCh38.p12 chr7: 73,337,330-73,337,331 RNU6-1080P, FKBP6
    nsv367236copy number variation1nstd6human NCBI35 chr7: 72,195,973-72,195,973 , GRCh37.p13 chr7|NW_003871064.1: 866,555-866,555 , GRCh37.p13 chr7: 72,751,322-72,751,322 , GRCh38.p12 chr7: 73,337,319-73,337,319 FKBP6, RNU6-1080P
    nsv365985copy number variation1nstd6human NCBI35 chr7: 72,195,972-72,195,972 , GRCh37.p13 chr7: 72,751,321-72,751,321 , GRCh37.p13 chr7|NW_003871064.1: 866,554-866,554 , GRCh38.p12 chr7: 73,337,318-73,337,318 FKBP6, RNU6-1080P
    nsv352869copy number variation1nstd6human NCBI35 chr7: 72,195,971-72,195,971 , GRCh37.p13 chr7|NW_003871064.1: 866,553-866,553 , GRCh37.p13 chr7: 72,751,320-72,751,320 , GRCh38.p12 chr7: 73,337,317-73,337,317 FKBP6, RNU6-1080P
    nsv5860998copy number variation2nstd209human GRCh38 chr7: 73,335,615-73,339,525 , GRCh37.p13 chr7|NW_003871064.1: 864,851-868,761 , GRCh37.p13 chr7: 72,749,617-72,753,528 FKBP6, RNU6-1080P
    nsv5856158copy number variation2nstd209human GRCh38 chr7: 73,336,215-73,337,214 , GRCh37.p13 chr7|NW_003871064.1: 865,451-866,450 , GRCh37.p13 chr7: 72,750,217-72,751,216 FKBP6, RNU6-1080P
    nsv4144784copy number variation1nstd166human GRCh37.p13 chr7: 72,745,614-72,754,503 , GRCh38.p12 chr7: 73,331,611-73,340,501 RNU6-1080P, FKBP6
    nsv1194474copy number variation2nstd113human NCBI36 chr7: 72,382,850-72,449,862 , GRCh37.p13 chr7|NW_003871064.1: 860,147-921,303 , GRCh37.p13 chr7: 72,744,914-72,806,397 , GRCh38.p12 chr7: 73,330,911-73,397,596 FKBP6, RNU6-1080P
    nsv1021613copy number variation4nstd100human NCBI36 chr7: 72,382,850-72,449,862 , GRCh37.p13 chr7|NW_003871064.1: 860,147-921,303 , GRCh37.p13 chr7: 72,744,914-72,806,397 , GRCh38.p12 chr7: 73,330,911-73,397,596 RNU6-1080P, FKBP6
    nsv1023935copy number variation1nstd100human NCBI36 chr7: 72,390,286-72,451,223 , GRCh37.p13 chr7: 72,752,350-72,806,397 , GRCh37.p13 chr7|NW_003871064.1: 867,583-921,303 , GRCh38.p12 chr7: 73,338,347-73,398,957 RNU6-1080P, FKBP6
    nsv1030211copy number variation1nstd100human NCBI36 chr7: 72,382,850-72,440,361 , GRCh37.p13 chr7|NW_003871064.1: 860,147-917,332 , GRCh37.p13 chr7: 72,744,914-72,802,425 , GRCh38.p12 chr7: 73,330,911-73,388,096 FKBP6, RNU6-1080P
    nsv538954copy number variation1nstd54human NCBI36 chr7: 72,382,850-72,449,862 , GRCh37.p13 chr7|NW_003871064.1: 860,147-921,303 , GRCh37.p13 chr7: 72,744,914-72,806,397 , GRCh38.p12 chr7: 73,330,911-73,397,596 FKBP6, RNU6-1080P
    nsv2499945short tandem repeat1nstd128human GRCh37 chr7: 72,752,028-72,752,048 , GRCh38.p12 chr7: 73,338,025-73,338,045 RNU6-1080P, FKBP6
    nsv3919679copy number variation1nstd102humanBenign NCBI36 chr7: 72,376,611-72,404,249 , GRCh38 chr7: 73,324,677-73,352,304 , GRCh37 chr7: 72,738,675-72,766,313 RNU6-1080P, FKBP6, 1 more genes
    nsv6636607copy number variation1nstd102humanUncertain significance GRCh37 chr7: 72,718,278-72,822,709 , GRCh38.p12 chr7: 73,304,281-73,408,379 TRIM50, NSUN5, 2 more genes
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