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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911447copy number variation1nstd209human GRCh38 chr11: 18,043,410-18,044,226 , GRCh37.p13 chr11: 18,064,957-18,065,773 TPH1
    nsv5721877mobile element insertion1nstd211human GRCh38 chr11: 18,032,100-18,032,100 , GRCh37.p13 chr11: 18,053,647-18,053,647 TPH1
    nsv5709860mobile element insertion2nstd211human GRCh38 chr11: 18,038,897-18,038,897 , GRCh37.p13 chr11: 18,060,444-18,060,444 TPH1
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5505909copy number variation1nstd206human GRCh38 chr11: 18,043,487-18,043,769 , GRCh37.p13 chr11: 18,065,034-18,065,316 TPH1
    nsv5503811copy number variation1nstd206human GRCh38 chr11: 18,030,003-18,033,018 , GRCh37.p13 chr11: 18,051,550-18,054,565 TPH1
    nsv5498284copy number variation1nstd206human GRCh38 chr11: 18,043,457-18,044,220 , GRCh37.p13 chr11: 18,065,004-18,065,767 TPH1
    nsv5404644mobile element insertion1nstd206human GRCh38 chr11: 18,038,897-18,038,948 , GRCh37.p13 chr11: 18,060,444-18,060,495 TPH1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5380720copy number variation1nstd102humanUncertain significance GRCh37 chr11: 17,552,691-19,213,995 , GRCh38.p12 chr11: 17,531,144-19,192,448 USH1C, HIGD1AP5, 53 more genes
    nsv5316634copy number variation1nstd204human GRCh37.p13 chr11: 18,066,958-18,072,179 , GRCh38.p13 chr11: 18,045,411-18,050,632 , TPH1
    nsv5250699copy number variation1nstd204human GRCh38.p13 chr11: 18,045,315-18,050,764 , GRCh37.p13 chr11: 18,066,862-18,072,311 , TPH1
    nsv5194037mobile element insertion1nstd203human GRCh38 chr11: 18,032,085-18,032,100 , GRCh37.p13 chr11: 18,053,632-18,053,647 TPH1
    nsv5181909mobile element insertion1nstd203human GRCh38 chr11: 18,032,089-18,032,100 , GRCh37.p13 chr11: 18,053,636-18,053,647 TPH1
    nsv4978441copy number variation1nstd200human GRCh38 chr11: 18,023,656-18,023,893 , GRCh37.p13 chr11: 18,045,203-18,045,440 TPH1
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
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