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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5697371mobile element insertion1nstd211human GRCh38 chr11: 114,572,601-114,572,601 , GRCh37.p13 chr11: 114,443,323-114,443,323 NXPE4, NXPE2
    nsv5599888copy number variation1nstd207human GRCh38 chr11: 114,577,013-114,577,074 , GRCh37.p13 chr11: 114,447,735-114,447,796 NXPE4, NXPE2
    nsv5540196insertion1nstd206human GRCh38 chr11: 114,577,056-114,577,062 , GRCh37.p13 chr11: 114,447,778-114,447,784 NXPE4, NXPE2
    nsv5513328copy number variation1nstd206human GRCh38 chr11: 114,591,466-114,591,526 , GRCh37.p13 chr11: 114,462,188-114,462,248 NXPE4, NXPE2
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5505847copy number variation1nstd206human GRCh38 chr11: 114,559,292-114,628,633 , GRCh37.p13 chr11: 114,430,014-114,499,355 NXPE4, NXPE1, 2 more genes
    nsv5493969copy number variation1nstd206human GRCh38 chr11: 114,587,124-114,632,798 , GRCh37.p13 chr11: 114,457,846-114,503,520 NXPE2, NXPE4
    nsv5418636mobile element insertion1nstd206human GRCh38 chr11: 114,572,601-114,572,652 , GRCh37.p13 chr11: 114,443,323-114,443,374 NXPE2, NXPE4
    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
    nsv5348312translocation1nstd200human GRCh38 chr11: 114,591,526-114,591,526 , GRCh38 chr11: 114,591,466-114,591,466 , GRCh37.p13 chr11: 114,462,248-114,462,248 , GRCh37.p13 chr11: 114,462,188-114,462,188 NXPE4, NXPE2
    nsv5035338inversion1nstd200human GRCh38 chr11: 114,039,980-117,481,226 , GRCh37.p13 chr11: 113,910,702-117,351,941 , LINC02703, 56 more genes
    nsv4980759copy number variation1nstd200human GRCh38 chr11: 114,573,454-114,573,649 , GRCh37.p13 chr11: 114,444,176-114,444,371 NXPE2, NXPE4
    nsv4980758copy number variation1nstd200human GRCh38 chr11: 114,530,888-114,735,901 , GRCh37.p13 chr11: 114,401,610-114,606,623 , NXPE2, 3 more genes
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4675323copy number variation1nstd102humanPathogenic GRCh37 chr11: 105,699,599-114,524,876 , GRCh38.p12 chr11: 105,828,873-114,654,154 RPSAP50, RNA5SP349, 155 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4507015mobile element insertion1nstd166human GRCh37.p13 chr11: 114,463,137-114,463,137 , GRCh38.p12 chr11: 114,592,415-114,592,415 NXPE4, NXPE2
    nsv4456659copy number variation1nstd102humanUncertain significance GRCh37 chr11: 110,969,076-114,578,509 , GRCh38.p12 chr11: 111,098,352-114,707,787 RPS29P19, PPP2R1B, 95 more genes
    nsv4455554copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202 LINC02732, LINC02698, 198 more genes
    nsv4209171copy number variation1nstd166human GRCh37.p13 chr11: 114,430,014-114,499,405 , GRCh38.p12 chr11: 114,559,292-114,628,683 NXPE1, NXPE2, 2 more genes
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