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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7042819inversion1nstd229human GRCh38 chr4: 89,525,733-90,153,148 , GRCh37.p13 chr4: 90,446,884-91,074,299 LOC105377329, SNCA, 4 more genes
    nsv6757501copy number variation1nstd229human GRCh38 chr4: 90,043,288-90,340,634 , GRCh37.p13 chr4: 90,964,439-91,261,785 CCSER1, LOC105377331
    nsv6754323copy number variation1nstd229human GRCh38 chr4: 90,065,198-90,065,403 , GRCh37.p13 chr4: 90,986,349-90,986,554 LOC105377331
    nsv6752327copy number variation1nstd229human GRCh38 chr4: 88,105,357-91,750,216 , GRCh37.p13 chr4: 89,026,509-92,671,367 HERC5, SNCA, 34 more genes
    nsv6752119copy number variation1nstd229human GRCh38 chr4: 90,058,628-90,058,720 , GRCh37.p13 chr4: 90,979,779-90,979,871 LOC105377331
    nsv6746823copy number variation1nstd229human GRCh38 chr4: 89,926,686-92,985,333 , GRCh37.p13 chr4: 90,847,837-93,906,484 LOC105377331, KRT19P6, 10 more genes
    nsv6743048copy number variation1nstd229human GRCh38 chr4: 89,976,891-90,214,471 , GRCh37.p13 chr4: 90,898,042-91,135,622 CCSER1, LOC105377331
    nsv6742606copy number variation1nstd229human GRCh38 chr4: 90,053,837-90,056,933 , GRCh37.p13 chr4: 90,974,988-90,978,084 LOC105377331
    nsv6387834copy number variation1nstd223human GRCh38 chr4: 90,046,301-90,047,300 , GRCh37.p13 chr4: 90,967,452-90,968,451 LOC105377331
    nsv6382640copy number variation1nstd223human GRCh38 chr4: 88,105,356-91,750,222 , GRCh37.p13 chr4: 89,026,508-92,671,373 PPM1K-DT, LOC105377327, 34 more genes
    nsv6382555copy number variation1nstd223human GRCh38 chr4: 90,043,287-90,340,633 , GRCh37.p13 chr4: 90,964,438-91,261,784 LOC105377331, CCSER1
    nsv6379085copy number variation1nstd223human GRCh38 chr4: 90,069,232-90,069,762 , GRCh37.p13 chr4: 90,990,383-90,990,913 LOC105377331
    nsv6313510copy number variation1nstd102humanPathogenic GRCh37 chr4: 75,737,340-91,131,156 , GRCh38.p12 chr4: 74,812,130-90,210,005 HIGD1AP13, CXCL11, 240 more genes
    nsv6313484copy number variation1nstd102humanPathogenic GRCh37 chr4: 79,780,152-94,873,225 , GRCh38.p12 chr4: 78,858,998-93,952,074 LOC105377329, LOC107986294, 166 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291420copy number variation1nstd102humanUncertain significance GRCh37 chr4: 90,943,592-91,196,145 , GRCh38.p12 chr4: 90,022,441-90,274,994 LOC105377331, CCSER1
    nsv6291249copy number variation1nstd102humanPathogenic GRCh37 chr4: 80,467,886-93,362,064 , GRCh38.p12 chr4: 79,546,732-92,440,913 HNRNPA3P13, LOC105377310, 155 more genes
    nsv6135047copy number variation1nstd213human GRCh37 chr4: 90,763,188-91,057,567 , GRCh38.p12 chr4: 89,842,037-90,136,416 MMRN1, CCSER1, 2 more genes
    nsv5907258copy number variation1nstd209human GRCh38 chr4: 87,165,110-92,683,258 , GRCh37.p13 chr4: 88,086,262-93,604,409 HSP90AB3P, SPP1, 61 more genes
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