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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979124inversion1nstd209human GRCh38 chr1: 231,183,716-231,183,930 , GRCh37.p13 chr1: 231,319,462-231,319,676 TRIM67-AS1, TRIM67
    nsv5972650inversion1nstd209human GRCh38 chr1: 229,174,728-232,234,598 , GRCh37.p13 chr1: 229,310,475-232,370,344 , ACTA1, 68 more genes
    nsv5971633inversion1nstd209human GRCh38 chr1: 229,416,331-231,831,980 , GRCh37.p13 chr1: 229,552,078-231,967,726 , ACTA1, 56 more genes
    nsv5962674insertion1nstd209human GRCh38 chr1: 231,202,070-231,202,070 , GRCh37.p13 chr1: 231,337,816-231,337,816 TRIM67
    nsv5948858insertion1nstd209human GRCh38 chr1: 231,167,319-231,167,319 , GRCh37.p13 chr1: 231,303,065-231,303,065 TRIM67
    nsv5883356copy number variation1nstd209human GRCh38 chr1: 231,162,133-231,162,362 , GRCh37.p13 chr1: 231,297,879-231,298,108 TRIM67
    nsv5871133copy number variation1nstd209human GRCh38 chr1: 231,210,927-231,211,049 , GRCh37.p13 chr1: 231,346,673-231,346,795 TRIM67
    nsv5870436copy number variation1nstd209human GRCh38 chr1: 231,184,145-231,186,248 , GRCh37.p13 chr1: 231,319,891-231,321,994 TRIM67-AS1, TRIM67
    nsv5829242copy number variation1nstd209human GRCh38 chr1: 231,221,926-231,223,253 , GRCh37.p13 chr1: 231,357,672-231,358,999 TRIM67, C1orf131
    nsv5829241copy number variation1nstd209human GRCh38 chr1: 231,184,091-231,186,090 , GRCh37.p13 chr1: 231,319,837-231,321,836 TRIM67, TRIM67-AS1
    nsv5721309mobile element insertion1nstd211human GRCh38 chr1: 231,221,240-231,221,240 , GRCh37.p13 chr1: 231,356,986-231,356,986 TRIM67
    nsv5676511mobile element insertion1nstd211human GRCh38 chr1: 231,208,851-231,208,851 , GRCh37.p13 chr1: 231,344,597-231,344,597 TRIM67
    nsv5619272insertion1nstd207human GRCh38 chr1: 231,202,070-231,202,070 , GRCh37.p13 chr1: 231,337,816-231,337,816 TRIM67
    nsv5576135copy number variation1nstd207human GRCh38 chr1: 231,167,319-231,167,624 , GRCh37.p13 chr1: 231,303,065-231,303,370 TRIM67
    nsv5568431copy number variation1nstd207human GRCh38 chr1: 231,210,927-231,211,049 , GRCh37.p13 chr1: 231,346,673-231,346,795 TRIM67
    nsv5567762copy number variation1nstd207human GRCh38 chr1: 231,184,145-231,186,248 , GRCh37.p13 chr1: 231,319,891-231,321,994 TRIM67-AS1, TRIM67
    nsv5555344inversion1nstd206human GRCh38 chr1: 231,183,711-231,183,949 , GRCh37.p13 chr1: 231,319,457-231,319,695 TRIM67-AS1, TRIM67
    nsv5449624copy number variation1nstd206human GRCh38 chr1: 231,162,136-231,162,363 , GRCh37.p13 chr1: 231,297,882-231,298,109 TRIM67
    nsv5447120copy number variation1nstd206human GRCh38 chr1: 231,167,330-231,167,625 , GRCh37.p13 chr1: 231,303,076-231,303,371 TRIM67
    nsv5445147copy number variation1nstd206human GRCh38 chr1: 230,482,037-231,277,187 , GRCh37.p13 chr1: 230,617,783-231,412,933 , LOC644006, 24 more genes
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