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 269

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099184copy number variation1nstd231human GRCh38.p12 chr1: 21,486,574-23,087,716 , GRCh37 chr1: 21,813,067-23,414,209 ALPL, C1QA, 36 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095589copy number variation1nstd102humanLikely benign GRCh37 chr1: 22,403,357-22,418,010 , GRCh38.p12 chr1: 22,076,864-22,091,517 CDC42
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7044318inversion1nstd229human GRCh38 chr1: 22,084,926-22,084,936 , GRCh37.p13 chr1: 22,411,419-22,411,429 CDC42
    nsv7041020inversion1nstd229human GRCh38 chr1: 22,006,431-22,106,241 , GRCh37.p13 chr1: 22,332,924-22,432,734 CDC42, CELA3A, 6 more genes
    nsv6647366copy number variation1nstd229human GRCh38 chr1: 22,073,029-22,078,196 , GRCh37.p13 chr1: 22,399,522-22,404,689 CDC42
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6646744copy number variation1nstd229human GRCh38 chr1: 21,707,701-22,087,100 , GRCh37.p13 chr1: 22,034,194-22,413,593 LDLRAD2, HSPG2, 13 more genes
    nsv6626098copy number variation1nstd224human GRCh37 chr1: 22,400,967-22,414,070 , GRCh38.p12 chr1: 22,074,474-22,087,577 CDC42
    nsv6543744inversion1nstd223human GRCh38 chr1: 22,061,237-22,061,595 , GRCh37.p13 chr1: 22,387,730-22,388,088 CDC42
    nsv6537751inversion1nstd223human GRCh38 chr1: 22,073,346-22,074,003 , GRCh37.p13 chr1: 22,399,839-22,400,496 CDC42
    nsv6322046copy number variation1nstd223human GRCh38 chr1: 22,089,347-22,089,551 , GRCh37.p13 chr1: 22,415,840-22,416,044 CDC42
    nsv6319052copy number variation1nstd223human GRCh38 chr1: 21,999,189-22,063,090 , GRCh37.p13 chr1: 22,325,682-22,389,583 CDC42, CELA3A, 5 more genes
    nsv6245583mobile element insertion1nstd215human GRCh38 chr1: 22,099,932-22,099,932 , GRCh37.p13 chr1: 22,426,425-22,426,425 CDC42
    nsv6225884insertion1nstd214human GRCh38 chr1: 22,082,073-22,082,073 , GRCh37.p13 chr1: 22,408,566-22,408,566 CDC42
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6133948copy number variation1nstd213human GRCh37 chr1: 17,280,000-26,950,001 , GRCh38.p12 chr1: 16,953,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv6133748copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,960,001 , GRCh38.p12 chr1: 16,943,505-26,633,510 ALPL, C1QA, 250 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