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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955041insertion1nstd209human GRCh38 chr2: 200,588,726-200,588,726 , GRCh37.p13 chr2: 201,453,449-201,453,449 AOX1
    nsv5950026insertion1nstd209human GRCh38 chr2: 200,657,190-200,657,190 , GRCh37.p13 chr2: 201,521,913-201,521,913 AOX1
    nsv5948307insertion1nstd209human GRCh38 chr2: 200,657,412-200,657,412 , GRCh37.p13 chr2: 201,522,135-201,522,135 AOX1
    nsv5674657mobile element insertion1nstd211human GRCh38 chr2: 200,634,361-200,634,361 , GRCh37.p13 chr2: 201,499,084-201,499,084 AOX1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5411967mobile element insertion1nstd206human GRCh38 chr2: 200,634,361-200,634,412 , GRCh37.p13 chr2: 201,499,084-201,499,135 AOX1
    nsv5334900translocation1nstd200human GRCh37 chr2: 201,530,634-201,530,634 , GRCh37 chr2: 201,530,724-201,530,724 , GRCh38.p12 chr2: 200,666,001-200,666,001 , GRCh38.p12 chr2: 200,665,911-200,665,911 AOX1
    nsv4910296copy number variation1nstd200human GRCh38 chr2: 200,665,911-200,666,001 , GRCh37.p13 chr2: 201,530,634-201,530,724 AOX1
    nsv4910295copy number variation1nstd200human GRCh38 chr2: 200,665,735-200,665,900 , GRCh37.p13 chr2: 201,530,458-201,530,623 AOX1
    nsv4910293copy number variation1nstd200human GRCh38 chr2: 200,561,587-200,584,444 , GRCh37.p13 chr2: 201,426,310-201,449,167 AOX1, SGO2
    nsv4795516copy number variation1nstd200human GRCh37 chr2: 201,534,012-201,540,726 , GRCh38.p12 chr2: 200,669,289-200,676,003 AOX1
    nsv4795515copy number variation1nstd200human GRCh37 chr2: 201,534,015-201,540,067 , GRCh38.p12 chr2: 200,669,292-200,675,344 AOX1
    nsv4795513copy number variation1nstd200human GRCh37 chr2: 201,426,310-201,449,167 , GRCh38.p12 chr2: 200,561,587-200,584,444 SGO2, AOX1
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4674597copy number variation1nstd102humanPathogenic GRCh37 chr2: 201,106,432-204,901,548 , GRCh38.p12 chr2: 200,241,709-204,036,825 KIAA2012-AS1, SNORD11, 113 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
    nsv4553650insertion1nstd166human GRCh37.p13 chr2: 201,461,043-201,461,043 , GRCh38.p12 chr2: 200,596,320-200,596,320 AOX1
    nsv4518538copy number variation1nstd166human GRCh37.p13 chr2: 201,410,102-201,639,125 , GRCh38.p12 chr2: 200,545,379-200,774,402 AOX1, SGO2, 5 more genes
    nsv4465778mobile element insertion1nstd166human GRCh37.p13 chr2: 201,522,540-201,522,540 , GRCh38.p12 chr2: 200,657,817-200,657,817 AOX1
    nsv4465777mobile element insertion1nstd166human GRCh37.p13 chr2: 201,518,701-201,518,701 , GRCh38.p12 chr2: 200,653,978-200,653,978 AOX1
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