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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5931678copy number variation1nstd209human GRCh38 chr14: 75,925,125-77,416,814 , GRCh37.p13 chr14: 76,391,468-77,883,157 TMED8, LOC105370573, 37 more genes
    nsv5704738mobile element insertion1nstd211human GRCh38 chr14: 76,766,067-76,766,067 , GRCh37.p13 chr14: 77,232,410-77,232,410 VASH1
    nsv5505173copy number variation1nstd206human GRCh38 chr14: 76,768,749-76,772,469 , GRCh37.p13 chr14: 77,235,092-77,238,812 VASH1
    nsv5495104copy number variation1nstd206human GRCh38 chr14: 76,761,860-76,761,925 , GRCh37.p13 chr14: 77,228,203-77,228,268 VASH1
    nsv5422645mobile element insertion1nstd206human GRCh38 chr14: 76,766,067-76,766,118 , GRCh37.p13 chr14: 77,232,410-77,232,461 VASH1
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004816copy number variation1nstd200human GRCh38 chr14: 76,494,566-76,823,810 , GRCh37.p13 chr14: 76,960,909-77,290,153 ESRRB, CYCSP1, 7 more genes
    nsv5004815copy number variation1nstd200human GRCh38 chr14: 76,477,007-76,782,389 , GRCh37.p13 chr14: 76,943,350-77,248,732 RPSAP3, ESRRB, 6 more genes
    nsv4847799copy number variation1nstd200human GRCh37 chr14: 76,943,350-77,248,732 , GRCh38.p12 chr14: 76,477,007-76,782,389 RPSAP3, ESRRB, 6 more genes
    nsv4504192mobile element insertion1nstd166human GRCh37.p13 chr14: 77,232,397-77,232,397 , GRCh38.p12 chr14: 76,766,054-76,766,054 VASH1
    nsv4456564copy number variation1nstd102humanUncertain significance GRCh37 chr14: 76,942,114-77,248,525 , GRCh38.p12 chr14: 76,475,771-76,782,182 RPSAP3, LOC105370576, 6 more genes
    nsv4376851copy number variation1nstd173human GRCh37 chr14: 77,042,465-77,865,966 , GRCh38.p12 chr14: 76,576,122-77,399,623 NGB, VASH1, 29 more genes
    nsv4367285copy number variation1nstd173human GRCh37 chr14: 77,039,093-77,865,966 , GRCh38.p12 chr14: 76,572,750-77,399,623 RPSAP3, NOXRED1, 29 more genes
    nsv4343237sequence alteration1nstd166human GRCh37.p13 chr14: 77,226,502-77,229,840 , GRCh38.p12 chr14: 76,760,159-76,763,497 VASH1
    nsv4225873copy number variation1nstd166human GRCh37.p13 chr14: 77,242,679-77,283,628 , GRCh38.p12 chr14: 76,776,336-76,817,285 ANGEL1, VASH1-AS1, 1 more genes
    nsv3923727copy number variation1nstd102humanPathogenic GRCh37 chr14: 70,028,816-82,441,728 , GRCh38 chr14: 69,562,099-81,975,384 , NCBI36 chr14: 69,098,569-81,511,481 CEP128, COX6CP11, 240 more genes
    nsv3923448copy number variation1nstd102humanPathogenic NCBI36 chr14: 73,413,528-77,578,518 , GRCh38 chr14: 73,877,072-78,042,422 , GRCh37 chr14: 74,343,775-78,508,765 ZC2HC1C, RPL21P10, 113 more genes
    nsv3922441copy number variation1nstd102humanPathogenic GRCh38 chr14: 75,489,052-79,610,332 , GRCh37 chr14: 75,955,395-80,076,675 , NCBI36 chr14: 75,025,148-79,146,428 IRF2BPL, LOC105370583, 69 more genes
    nsv3922094copy number variation1nstd102humanPathogenic GRCh38 chr14: 73,655,772-106,879,298 , GRCh37 chr14: 74,122,475-107,287,505 , NCBI36 chr14: 73,192,228-106,358,550 LOC105370614, LOC105370617, 849 more genes
    nsv3921740copy number variation1nstd102humanLikely benign NCBI36 chr14: 75,855,447-76,380,814 , GRCh38 chr14: 76,319,351-76,844,718 , GRCh37 chr14: 76,785,694-77,311,061 RPSAP3, LRRC74A, 8 more genes
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