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Items: 1 to 20 of 281

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949823insertion1nstd209human GRCh38 chr6: 70,249,172-70,249,172 , GRCh37.p13 chr6: 70,958,875-70,958,875 COL9A1
    nsv5893197copy number variation1nstd209human GRCh38 chr6: 70,257,954-70,258,047 , GRCh37.p13 chr6: 70,967,657-70,967,750 COL9A1
    nsv5887723copy number variation1nstd209human GRCh38 chr6: 70,264,868-70,276,211 , GRCh37.p13 chr6: 70,974,571-70,985,914 COL9A1
    nsv5846064copy number variation1nstd209human GRCh38 chr6: 70,264,810-70,276,053 , GRCh37.p13 chr6: 70,974,513-70,985,756 COL9A1
    nsv5687173mobile element insertion2nstd211human GRCh38 chr6: 70,249,187-70,249,187 , GRCh37.p13 chr6: 70,958,890-70,958,890 COL9A1
    nsv5681990mobile element insertion1nstd211human GRCh38 chr6: 70,263,387-70,263,387 , GRCh37.p13 chr6: 70,973,090-70,973,090 COL9A1
    nsv5677791mobile element insertion2nstd211human GRCh38 chr6: 70,269,560-70,269,560 , GRCh37.p13 chr6: 70,979,263-70,979,263 COL9A1
    nsv5626891insertion1nstd207human GRCh38 chr6: 70,249,172-70,249,172 , GRCh37.p13 chr6: 70,958,875-70,958,875 COL9A1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5470560copy number variation1nstd206human GRCh38 chr6: 70,231,275-70,231,928 , GRCh37.p13 chr6: 70,940,978-70,941,631 COL9A1
    nsv5466062copy number variation1nstd206human GRCh38 chr6: 70,267,561-70,267,617 , GRCh37.p13 chr6: 70,977,264-70,977,320 COL9A1
    nsv5403320mobile element insertion1nstd206human GRCh38 chr6: 70,269,560-70,269,611 , GRCh37.p13 chr6: 70,979,263-70,979,314 COL9A1
    nsv5399231mobile element insertion1nstd206human GRCh38 chr6: 70,263,387-70,263,438 , GRCh37.p13 chr6: 70,973,090-70,973,141 COL9A1
    nsv5398255mobile element insertion1nstd206human GRCh38 chr6: 70,249,187-70,249,238 , GRCh37.p13 chr6: 70,958,890-70,958,941 COL9A1
    nsv5381532copy number variation1nstd102humanUncertain significance GRCh37 chr6: 69,802,503-71,012,627 , GRCh38.p12 chr6: 69,092,611-70,302,924 COL9A1, GAPDHP42, 5 more genes
    nsv5117067mobile element insertion1nstd203human GRCh38 chr6: 70,249,173-70,249,187 , GRCh37.p13 chr6: 70,958,876-70,958,890 COL9A1
    nsv5114348mobile element insertion1nstd203human GRCh38 chr6: 70,249,176-70,249,187 , GRCh37.p13 chr6: 70,958,879-70,958,890 COL9A1
    nsv5114068mobile element insertion1nstd203human GRCh38 chr6: 70,249,171-70,249,183 , GRCh37.p13 chr6: 70,958,874-70,958,886 COL9A1
    nsv5111042mobile element insertion1nstd203human GRCh38 chr6: 70,263,372-70,263,384 , GRCh37.p13 chr6: 70,973,075-70,973,087 COL9A1
    nsv5108584mobile element insertion1nstd203human GRCh38 chr6: 70,249,172-70,249,187 , GRCh37.p13 chr6: 70,958,875-70,958,890 COL9A1
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