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Items: 1 to 20 of 286

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948955insertion1nstd209human GRCh38 chr5: 122,330,117-122,330,117 , GRCh37.p13 chr5: 121,665,812-121,665,812 SNCAIP
    nsv5893016copy number variation1nstd209human GRCh38 chr5: 122,357,887-122,358,767 , GRCh37.p13 chr5: 121,693,582-121,694,462 SNCAIP
    nsv5714378mobile element insertion1nstd211human GRCh38 chr5: 122,359,047-122,359,047 , GRCh37.p13 chr5: 121,694,742-121,694,742 SNCAIP
    nsv5471611copy number variation1nstd206human GRCh38 chr5: 122,321,468-122,327,046 , GRCh37.p13 chr5: 121,657,163-121,662,741 SNCAIP
    nsv5469708copy number variation1nstd206human GRCh38 chr5: 122,393,615-122,398,996 , GRCh37.p13 chr5: 121,729,310-121,734,691 SNCAIP
    nsv5460330copy number variation1nstd206human GRCh38 chr5: 122,388,823-122,388,908 , GRCh37.p13 chr5: 121,724,518-121,724,603 SNCAIP
    nsv5456998copy number variation1nstd206human GRCh38 chr5: 122,414,056-122,414,400 , GRCh37.p13 chr5: 121,749,751-121,750,095 SNCAIP
    nsv5377998translocation1nstd200human GRCh38 chr5: 122,414,081-122,414,081 , GRCh38 chr5: 122,414,380-122,414,380 , GRCh37.p13 chr5: 121,749,776-121,749,776 , GRCh37.p13 chr5: 121,750,075-121,750,075 SNCAIP
    nsv5377704translocation1nstd200human GRCh38 chr5: 122,335,030-122,335,030 , GRCh38 chr4: 151,811,275-151,811,275 , GRCh37.p13 chr4: 152,732,427-152,732,427 , GRCh37.p13 chr5: 121,670,725-121,670,725 LOC105377488, SNCAIP
    nsv5330492translocation1nstd200human GRCh37 chr5: 121,678,734-121,678,734 , GRCh37 chr5: 121,678,671-121,678,671 , GRCh38.p12 chr5: 122,343,039-122,343,039 , GRCh38.p12 chr5: 122,342,976-122,342,976 SNCAIP
    nsv5324167translocation1nstd204human GRCh38.p13 chr5: 122,342,976-122,342,976 , GRCh38.p13 chr5: 122,343,039-122,343,039 , GRCh37.p13 chr5: 121,678,734-121,678,734 , GRCh37.p13 chr5: 121,678,671-121,678,671 SNCAIP
    nsv5239190copy number variation1nstd204human GRCh38.p13 chr5: 122,378,101-122,379,000 , GRCh37.p13 chr5: 121,713,796-121,714,695 SNCAIP
    nsv5172975mobile element insertion1nstd203human GRCh38 chr5: 122,333,199-122,333,199 , GRCh37.p13 chr5: 121,668,894-121,668,894 SNCAIP
    nsv5089011mobile element insertion1nstd203human GRCh38 chr5: 122,330,117-122,330,139 , GRCh37.p13 chr5: 121,665,812-121,665,834 SNCAIP
    nsv5085872mobile element insertion1nstd203human GRCh38 chr5: 122,447,370-122,447,377 , GRCh37.p13 chr5: 121,783,065-121,783,072 MGC32805, SNCAIP
    nsv5082829mobile element insertion1nstd203human GRCh38 chr5: 122,330,139-122,330,162 , GRCh37.p13 chr5: 121,665,834-121,665,857 SNCAIP
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4945010copy number variation1nstd200human GRCh38 chr5: 122,414,059-122,414,402 , GRCh37.p13 chr5: 121,749,754-121,750,097 SNCAIP
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