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Items: 1 to 20 of 160

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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
    nsv7137046copy number variation1nstd102humanPathogenic GRCh38.p12 chr4: 89,247,780-89,953,418 , GRCh37 chr4: 90,168,931-90,874,569 SNCA, MMRN1, 4 more genes
    nsv7137029copy number variation2nstd102humanPathogenic GRCh38 chr4: 89,724,098-89,934,809 , GRCh37.p13 chr4: 90,645,249-90,855,960 SNCA, MMRN1, 1 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
    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
    nsv6741407copy number variation1nstd229human GRCh38 chr4: 89,831,507-89,834,872 , GRCh37.p13 chr4: 90,752,658-90,756,023 SNCA, SNCA-AS1
    nsv6574395inversion1nstd223human GRCh38 chr4: 87,923,661-89,968,732 , GRCh37.p13 chr4: 88,844,813-90,889,883 LOC102723458, LOC105377329, 33 more genes
    nsv6556594inversion1nstd223human GRCh38 chr4: 87,923,653-89,968,726 , GRCh37.p13 chr4: 88,844,805-90,889,877 LOC105377326, SNCA, 33 more genes
    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
    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
    nsv6311923copy number variation1nstd102humanPathogenic GRCh37 chr4: 90,647,779-90,756,818 , GRCh38.p12 chr4: 89,726,628-89,835,667 SNCA, SNCA-AS1
    nsv6311732copy number variation1nstd102humanUncertain significance GRCh37 chr4: 90,647,315-90,756,828 , GRCh38.p12 chr4: 89,726,164-89,835,677 SNCA, SNCA-AS1
    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
    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
    nsv6291054copy number variation1nstd102humannot provided GRCh37 chr4: 90,647,779-90,756,863 , GRCh38.p12 chr4: 89,726,628-89,835,712 SNCA-AS1, SNCA
    nsv6135366copy number variation1nstd213human GRCh37 chr4: 90,520,000-90,760,001 , GRCh38.p12 chr4: 89,598,849-89,838,850 SNCA, SNCA-AS1, 1 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
    nsv5896016copy number variation1nstd209human GRCh38 chr4: 89,841,068-89,841,266 , GRCh37.p13 chr4: 90,762,219-90,762,417 SNCA-AS1
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