U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 195

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6996488copy number variation1nstd229human GRCh38 chr17: 40,629,706-40,629,775 , GRCh37.p13 chr17: 38,785,958-38,786,027 SMARCE1
    nsv6989153copy number variation1nstd229human GRCh38 chr17: 40,635,341-40,635,704 , GRCh37.p13 chr17: 38,791,593-38,791,956 SMARCE1
    nsv6985080copy number variation1nstd229human GRCh38 chr17: 40,639,240-40,639,413 , GRCh37.p13 chr17: 38,795,492-38,795,665 SMARCE1
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6508523copy number variation1nstd223human GRCh38 chr17: 40,636,601-40,637,200 , GRCh37.p13 chr17: 38,792,853-38,793,452 SMARCE1
    nsv6507886copy number variation1nstd223human GRCh38 chr17: 40,636,970-40,637,673 , GRCh37.p13 chr17: 38,793,222-38,793,925 SMARCE1
    nsv6310381copy number variation1nstd102humanUncertain significance GRCh37 chr17: 38,798,697-38,804,103 , GRCh38.p12 chr17: 40,642,445-40,647,851 SMARCE1
    nsv6133356copy number variation1nstd213human GRCh37 chr17: 38,650,000-38,780,001 , GRCh38.p12 chr17: 40,493,748-40,623,749 CCR7, SMARCE1, 3 more genes
    nsv6133056copy number variation1nstd213human GRCh37 chr17: 36,400,000-39,740,001 , GRCh38.p12 chr17: 38,545,381-41,583,749 CACNB1, CDC6, 176 more genes
    nsv5729770mobile element insertion1nstd211human GRCh38 chr17: 40,624,563-40,624,563 , GRCh37.p13 chr17: 38,780,815-38,780,815 SMARCE1
    nsv5706864mobile element insertion1nstd211human GRCh38 chr17: 40,636,771-40,636,771 , GRCh37.p13 chr17: 38,793,023-38,793,023 SMARCE1
    nsv5554584mobile element insertion1nstd206human GRCh38 chr17: 40,624,563-40,624,614 , GRCh37.p13 chr17: 38,780,815-38,780,866 SMARCE1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5518229copy number variation1nstd206human GRCh38 chr17: 40,636,041-40,636,137 , GRCh37.p13 chr17: 38,792,293-38,792,389 SMARCE1
    nsv5418605mobile element insertion1nstd206human GRCh38 chr17: 40,636,771-40,636,822 , GRCh37.p13 chr17: 38,793,023-38,793,074 SMARCE1
    nsv5153057mobile element insertion1nstd203human GRCh38 chr17: 40,641,923-40,641,939 , GRCh37.p13 chr17: 38,798,175-38,798,191 SMARCE1
    nsv4681542copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr17: 38,785,037-38,804,103 , GRCh38.p12 chr17: 40,628,785-40,647,851 SMARCE1
    nsv4679355copy number variation1nstd189human GRCh37.p13 chr17: 38,659,900-39,414,647 , GRCh38.p12 chr17: 40,503,648-41,258,395 , CCR7, 54 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center