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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7051957inversion1nstd229human GRCh38 chr3: 100,950,457-102,238,704 , GRCh37.p13 chr3: 100,669,301-101,957,548 RPL24, ACTR3P3, 22 more genes
    nsv6709812copy number variation1nstd229human GRCh38 chr3: 101,563,252-101,563,295 , GRCh37.p13 chr3: 101,282,096-101,282,139 TRMT10C
    nsv6704084copy number variation1nstd229human GRCh38 chr3: 101,562,004-101,564,768 , GRCh37.p13 chr3: 101,280,848-101,283,612 TRMT10C
    nsv6537526inversion1nstd223human GRCh38 chr3: 94,859,299-102,665,887 , GRCh37.p13 chr3: 94,578,143-102,384,731 OR5AC4P, LOC105373996, 112 more genes
    nsv6373900copy number variation1nstd223human GRCh38 chr3: 101,566,917-101,568,974 , GRCh37.p13 chr3: 101,285,761-101,287,818 TRMT10C
    nsv6370717copy number variation1nstd223human GRCh38 chr3: 101,560,101-101,561,000 , GRCh37.p13 chr3: 101,278,945-101,279,844 TRMT10C
    nsv6313516copy number variation1nstd102humanUncertain significance GRCh37 chr3: 101,191,611-101,938,521 , GRCh38.p12 chr3: 101,472,767-102,219,677 CEP97, ZBTB11-AS1, 15 more genes
    nsv6311848copy number variation1nstd102humanUncertain significance GRCh37 chr3: 101,283,626-101,284,837 , GRCh38.p12 chr3: 101,564,782-101,565,993 TRMT10C
    nsv6311846copy number variation1nstd102humanPathogenic GRCh37 chr3: 100,945,813-101,484,395 , GRCh38.p12 chr3: 101,226,969-101,765,551 IMPG2, ZBTB11-AS1, 15 more genes
    nsv6311433copy number variation1nstd102humanUncertain significance GRCh37 chr3: 100,945,813-101,284,837 , GRCh38.p12 chr3: 101,226,969-101,565,993 SENP7, FAM136CP, 5 more genes
    nsv6076054insertion1nstd212human GRCh38 chr3: 101,560,799-101,560,799 , GRCh37.p13 chr3: 101,279,643-101,279,643 TRMT10C
    nsv5991173copy number variation1nstd212human GRCh38 chr3: 101,562,005-101,564,769 , GRCh37.p13 chr3: 101,280,849-101,283,613 TRMT10C
    nsv5962972insertion1nstd209human GRCh38 chr3: 101,560,799-101,560,799 , GRCh37.p13 chr3: 101,279,643-101,279,643 TRMT10C
    nsv5893265copy number variation1nstd209human GRCh38 chr3: 101,562,002-101,564,767 , GRCh37.p13 chr3: 101,280,846-101,283,611 TRMT10C
    nsv5619394insertion1nstd207human GRCh38 chr3: 101,560,799-101,560,799 , GRCh37.p13 chr3: 101,279,643-101,279,643 TRMT10C
    nsv5440172copy number variation1nstd206human GRCh38 chr3: 101,562,004-101,564,768 , GRCh37.p13 chr3: 101,280,848-101,283,612 TRMT10C
    nsv5377112translocation1nstd200human GRCh38 chr2: 77,350,662-77,350,662 , GRCh38 chr3: 101,561,133-101,561,133 , GRCh37.p13 chr2: 77,577,788-77,577,788 , GRCh37.p13 chr3: 101,279,977-101,279,977 TRMT10C, LRRTM4
    nsv5373479translocation1nstd200human GRCh38 chr3: 101,566,262-101,566,262 , GRCh38 chr1: 209,930,988-209,930,988 , GRCh37.p13 chr1: 210,104,333-210,104,333 , GRCh37.p13 chr3: 101,285,106-101,285,106 TRMT10C
    nsv5373476translocation1nstd200human GRCh38 chr1: 209,930,987-209,930,987 , GRCh38 chr3: 101,565,264-101,565,264 , GRCh37.p13 chr1: 210,104,332-210,104,332 , GRCh37.p13 chr3: 101,284,108-101,284,108 TRMT10C
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