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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098859copy number variation1nstd102humanUncertain significance GRCh37 chr4: 169,669,584-172,013,457 , GRCh38.p12 chr4: 168,748,433-171,092,306 RNY4P17, LOC105377529, 27 more genes
    nsv7056217inversion1nstd229human GRCh38 chr4: 166,607,935-172,500,612 , GRCh37.p13 chr4: 167,529,086-173,421,763 DDX60, LOC105377529, 50 more genes
    nsv7054944inversion1nstd229human GRCh38 chr4: 169,647,111-171,933,053 , GRCh37.p13 chr4: 170,568,262-172,854,204 PTGES3P3, LOC402192, 23 more genes
    nsv7038664inversion1nstd229human GRCh38 chr4: 170,091,988-172,217,645 , GRCh37.p13 chr4: 171,013,139-173,138,796 MIR6082, LINC02504, 14 more genes
    nsv6757256copy number variation1nstd229human GRCh38 chr4: 170,064,405-170,067,528 , GRCh37.p13 chr4: 170,985,556-170,988,679 LOC107986326, AADAT
    nsv6755882copy number variation1nstd229human GRCh38 chr4: 170,084,661-170,085,913 , GRCh37.p13 chr4: 171,005,812-171,007,064 AADAT
    nsv6754173copy number variation1nstd229human GRCh38 chr4: 169,732,023-170,107,311 , GRCh37.p13 chr4: 170,653,174-171,028,462 PTGES3P3, LOC402192, 8 more genes
    nsv6750704copy number variation1nstd229human GRCh38 chr4: 169,991,201-170,066,000 , GRCh37.p13 chr4: 170,912,352-170,987,151 AADAT, MFAP3L, 1 more genes
    nsv6750334copy number variation1nstd229human GRCh38 chr4: 170,080,701-170,083,000 , GRCh37.p13 chr4: 171,001,852-171,004,151 AADAT
    nsv6747869copy number variation1nstd229human GRCh38 chr4: 169,923,980-170,085,263 , GRCh37.p13 chr4: 170,845,131-171,006,414 AADAT, LOC105377530, 3 more genes
    nsv6744752copy number variation1nstd229human GRCh38 chr4: 170,077,518-170,077,847 , GRCh37.p13 chr4: 170,998,669-170,998,998 AADAT
    nsv6741318copy number variation1nstd229human GRCh38 chr4: 170,078,159-170,983,868 , GRCh37.p13 chr4: 170,999,310-171,905,019 HSP90AA6P, RNU6ATAC13P, 5 more genes
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6629209copy number variation1nstd224human GRCh37 chr4: 170,909,908-171,206,696 , GRCh38.p12 chr4: 169,988,757-170,285,545 MFAP3L, LOC107986326, 3 more genes
    nsv6570050inversion1nstd223human GRCh38 chr4: 169,780,525-178,315,900 , GRCh37.p13 chr4: 170,701,676-179,237,054 LOC101928409, LOC100131553, 91 more genes
    nsv6395360copy number variation1nstd223human GRCh38 chr4: 170,090,301-170,096,400 , GRCh37.p13 chr4: 171,011,452-171,017,551 AADAT
    nsv6391417copy number variation1nstd223human GRCh38 chr4: 170,088,901-170,090,500 , GRCh37.p13 chr4: 171,010,052-171,011,651 AADAT
    nsv6390689copy number variation1nstd223human GRCh38 chr4: 170,064,115-170,064,570 , GRCh37.p13 chr4: 170,985,266-170,985,721 LOC107986326, AADAT
    nsv6385162copy number variation1nstd223human GRCh38 chr4: 170,086,801-170,093,900 , GRCh37.p13 chr4: 171,007,952-171,015,051 AADAT
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