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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
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5439539copy number variation1nstd206human GRCh38 chr2: 210,027,874-210,027,929 , GRCh37.p13 chr2: 210,892,598-210,892,653 KANSL1L, KANSL1L-AS1
    nsv5366802translocation1nstd200human GRCh38 chr2: 210,050,933-210,050,933 , GRCh38 chr2: 210,049,833-210,049,833 , GRCh37.p13 chr2: 210,914,557-210,914,557 , GRCh37.p13 chr2: 210,915,657-210,915,657 KANSL1L, KANSL1L-AS1
    nsv5366801translocation1nstd200human GRCh38 chr2: 210,047,200-210,047,200 , GRCh38 chr2: 210,049,928-210,049,928 , GRCh37.p13 chr2: 210,911,924-210,911,924 , GRCh37.p13 chr2: 210,914,652-210,914,652 KANSL1L-AS1, KANSL1L
    nsv5209563copy number variation1nstd204human GRCh38.p13 chr2: 210,038,001-210,044,500 , GRCh37.p13 chr2: 210,902,725-210,909,224 KANSL1L, KANSL1L-AS1
    nsv5202505copy number variation1nstd204human GRCh38.p13 chr2: 210,035,901-210,040,600 , GRCh37.p13 chr2: 210,900,625-210,905,324 KANSL1L, KANSL1L-AS1
    nsv5074441mobile element insertion1nstd203human GRCh38 chr2: 210,042,153-210,042,164 , GRCh37.p13 chr2: 210,906,877-210,906,888 KANSL1L, KANSL1L-AS1
    nsv4916590copy number variation1nstd200human GRCh38 chr2: 210,047,198-210,050,935 , GRCh37.p13 chr2: 210,911,922-210,915,659 KANSL1L-AS1, KANSL1L
    nsv4916589copy number variation1nstd200human GRCh38 chr2: 210,037,977-210,039,687 , GRCh37.p13 chr2: 210,902,701-210,904,411 KANSL1L, KANSL1L-AS1
    nsv4916588copy number variation1nstd200human GRCh38 chr2: 210,028,373-210,029,190 , GRCh37.p13 chr2: 210,893,097-210,893,914 KANSL1L-AS1, KANSL1L
    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
    nsv4728545copy number variation1nstd102humanPathogenic GRCh37 chr2: 204,445,619-212,580,788 , GRCh38.p12 chr2: 203,580,896-211,716,063 FASTKD2, MYL6BP1, 110 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
    nsv4568959sequence alteration1nstd166human GRCh37.p13 chr2: 210,914,897-210,915,533 , GRCh38.p12 chr2: 210,050,173-210,050,809 KANSL1L, KANSL1L-AS1
    nsv4436532copy number variation1nstd102humanPathogenic GRCh37 chr2: 188,926,928-225,298,653 , GRCh38.p12 chr2: 188,062,201-224,433,936 MARS2, KRT18P19, 575 more genes
    nsv4435891copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487 XRCC5, LINC01173, 494 more genes
    nsv4316119inversion1nstd166human GRCh37.p13 chr2: 187,130,612-218,396,189 , GRCh38.p12 chr2: 186,265,885-217,531,466 , ACADL, 453 more genes
    nsv4315068inversion1nstd166human GRCh37.p13 chr2: 208,775,197-231,007,646 , GRCh38.p12 chr2: 207,910,473-230,142,930 , BCS1L, 344 more genes
    nsv4087382copy number variation1nstd166human GRCh37.p13 chr2: 210,906,224-210,906,897 , GRCh38.p12 chr2: 210,041,500-210,042,173 KANSL1L-AS1, KANSL1L
    nsv4081761copy number variation1nstd166human GRCh37.p13 chr2: 210,898,509-210,901,195 , GRCh38.p12 chr2: 210,033,785-210,036,471 KANSL1L-AS1, KANSL1L
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