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Results: 1 to 20 of 54

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Number of Variants: 20

Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
nsv993435copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr11: 46,442,505-46,749,922 , GRCh38 chr11: 46,420,955-46,728,372 , NCBI36 (hg18) chr11: 46,399,081-46,706,498 MIR3160-2, MIR3160-1, 6 more genes
nsv984845copy number variation3nstd11humannot provided GRCh37 (hg19) chr11: 198,510-134,944,770 , NCBI36 (hg18) chr11: 188,510-134,449,982 , GRCh38 chr11: 198,510-135,074,876 TRNAF1, ANO1-AS2, 1508 more genes
esv3425366copy number variation2estd59human NCBI36 (hg18) chr11: 46,637,633-46,637,925 , GRCh37 (hg19) chr11: 46,681,057-46,681,349 , GRCh38 chr11: 46,659,507-46,659,799 ATG13
esv2890061insertion1estd209human GRCh37 (hg19) chr11: 46,644,988-46,644,988 , GRCh38 chr11: 46,623,438-46,623,438 ATG13
esv2890062insertion1estd209human GRCh37 (hg19) chr11: 46,663,310-46,663,310 , GRCh38 chr11: 46,641,760-46,641,760 ATG13
esv3149997copy number variation1estd209human GRCh37 (hg19) chr11: 46,688,466-46,688,468 , GRCh38 chr11: 46,666,916-46,666,918 ATG13
esv3149996copy number variation1estd209human GRCh37 (hg19) chr11: 46,668,007-46,668,013 , GRCh38 chr11: 46,646,457-46,646,463 ATG13
esv3149995copy number variation1estd209human GRCh37 (hg19) chr11: 46,638,886-46,638,888 , GRCh38 chr11: 46,617,336-46,617,338 HARBI1, ATG13
esv3149998copy number variation1estd209human GRCh37 (hg19) chr11: 46,694,313-46,694,315 , GRCh38 chr11: 46,672,763-46,672,765 ATG13
nsv948795copy number variation1nstd85human GRCh37 (hg19) chr11: 211,447-50,635,122 , NCBI35 (hg17) chr11: 201,447-50,591,698 , GRCh38 chr11: 211,447-50,675,951 MIR675, MRVI1-AS1, 516 more genes
nsv916880copy number variation1nstd37humanLikely pathogenic NCBI36 (hg18) chr11: 42,705,681-49,113,863 , GRCh37 (hg19) chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735 MIR670, MIR3160-2, 83 more genes
nsv897321copy number variation1nstd71human NCBI36 (hg18) chr11: 46,472,478-46,629,920 , GRCh37 (hg19) chr11: 46,515,902-46,673,344 , GRCh38 chr11: 46,494,352-46,651,794 HARBI1, AMBRA1, 1 more genes
esv1777143insertion1estd22human NCBI36 (hg18) chr11: 46,641,413-46,641,413 , GRCh37 (hg19) chr11: 46,684,837-46,684,837 , GRCh38 chr11: 46,663,287-46,663,287 ATG13
esv1652343insertion1estd22human NCBI36 (hg18) chr11: 46,638,526-46,638,526 , GRCh37 (hg19) chr11: 46,681,950-46,681,950 , GRCh38 chr11: 46,660,400-46,660,400 ATG13
esv1640922insertion1estd22human NCBI36 (hg18) chr11: 46,619,900-46,619,900 , GRCh37 (hg19) chr11: 46,663,324-46,663,324 , GRCh38 chr11: 46,641,774-46,641,774 ATG13
esv1630358copy number variation1estd22human NCBI36 (hg18) chr11: 46,624,601-46,624,607 , GRCh37 (hg19) chr11: 46,668,025-46,668,031 , GRCh38 chr11: 46,646,475-46,646,481 ATG13
esv1312812copy number variation1estd22human NCBI36 (hg18) chr11: 46,625,419-46,625,432 , GRCh37 (hg19) chr11: 46,668,843-46,668,856 , GRCh38 chr11: 46,647,293-46,647,306 ATG13
esv1301092insertion1estd22human NCBI36 (hg18) chr11: 46,620,450-46,620,450 , GRCh37 (hg19) chr11: 46,663,874-46,663,874 , GRCh38 chr11: 46,642,324-46,642,324 ATG13
esv1151329copy number variation1estd22human NCBI36 (hg18) chr11: 46,650,889-46,650,891 , GRCh37 (hg19) chr11: 46,694,313-46,694,315 , GRCh38 chr11: 46,672,763-46,672,765 ATG13
esv1145523insertion1estd22human NCBI36 (hg18) chr11: 46,638,553-46,638,553 , GRCh37 (hg19) chr11: 46,681,977-46,681,977 , GRCh38 chr11: 46,660,427-46,660,427 ATG13

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