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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052737inversion1nstd229human GRCh38 chr4: 124,487,719-129,666,522 , GRCh37.p13 chr4: 125,408,874-130,587,677 H3P15, ANKRD50, 36 more genes
    nsv7043630inversion1nstd229human GRCh38 chr4: 127,283,753-130,065,798 , GRCh37.p13 chr4: 128,204,908-130,986,953 SCLT1, JADE1, 30 more genes
    nsv6748101copy number variation1nstd229human GRCh38 chr4: 129,107,154-129,107,522 , GRCh37.p13 chr4: 130,028,309-130,028,677 C4orf33
    nsv6744205copy number variation1nstd229human GRCh38 chr4: 129,095,559-129,098,279 , GRCh37.p13 chr4: 130,016,714-130,019,434 C4orf33
    nsv6743236copy number variation1nstd229human GRCh38 chr4: 129,108,401-129,139,700 , GRCh37.p13 chr4: 130,029,556-130,060,855 C4orf33, CDRT15P11, 1 more genes
    nsv6390964copy number variation1nstd223human GRCh38 chr4: 129,111,644-129,112,119 , GRCh37.p13 chr4: 130,032,799-130,033,274 C4orf33
    nsv6388822copy number variation1nstd223human GRCh38 chr4: 129,105,601-129,107,500 , GRCh37.p13 chr4: 130,026,756-130,028,655 C4orf33
    nsv6382181copy number variation1nstd223human GRCh38 chr4: 129,101,001-129,102,000 , GRCh37.p13 chr4: 130,022,156-130,023,155 C4orf33
    nsv6378195copy number variation1nstd223human GRCh38 chr4: 129,108,001-129,108,444 , GRCh37.p13 chr4: 130,029,156-130,029,599 C4orf33
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6311903copy number variation1nstd102humanPathogenic GRCh37 chr4: 129,960,176-130,014,258 , GRCh38.p12 chr4: 129,039,021-129,093,103 SCLT1, C4orf33
    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
    nsv6290862copy number variation1nstd102humanUncertain significance GRCh37 chr4: 129,938,155-130,059,879 , GRCh38.p12 chr4: 129,017,000-129,138,724 ZSWIM5P3, SCLT1, 2 more genes
    nsv6290265copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113 LOC105379404, IL21-AS1, 218 more genes
    nsv6135057copy number variation1nstd213human GRCh37 chr4: 129,820,000-130,190,001 , GRCh38.p12 chr4: 128,898,845-129,268,846 SCLT1, C4orf33, 2 more genes
    nsv6135056copy number variation1nstd213human GRCh37 chr4: 129,810,000-130,520,001 , GRCh38.p12 chr4: 128,888,845-129,598,846 SCLT1, C4orf33, 4 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv5618172insertion1nstd207human GRCh38 chr4: 129,115,819-129,115,819 , GRCh37.p13 chr4: 130,036,974-130,036,974 C4orf33
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
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