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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5694182mobile element insertion2nstd211human GRCh38 chr1: 157,130,782-157,130,782 , GRCh37.p13 chr1: 157,100,574-157,100,574 ETV3
    nsv5418489copy number variation1nstd206human GRCh38 chr1: 157,136,009-157,136,173 , GRCh37.p13 chr1: 157,105,801-157,105,965 ETV3
    nsv5413813mobile element insertion1nstd206human GRCh38 chr1: 157,130,782-157,130,833 , GRCh37.p13 chr1: 157,100,574-157,100,625 ETV3
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5370955translocation1nstd200human GRCh38 chr1: 157,136,108-157,136,108 , GRCh38 chr1: 157,137,027-157,137,027 , GRCh37.p13 chr1: 157,105,900-157,105,900 , GRCh37.p13 chr1: 157,106,819-157,106,819 ETV3
    nsv5370950translocation1nstd200human GRCh38 chr1: 157,137,040-157,137,040 , GRCh38 chr1: 157,135,935-157,135,935 , GRCh37.p13 chr1: 157,105,727-157,105,727 , GRCh37.p13 chr1: 157,106,832-157,106,832 ETV3
    nsv4897616copy number variation1nstd200human GRCh38 chr1: 157,136,009-157,136,173 , GRCh37.p13 chr1: 157,105,801-157,105,965 ETV3
    nsv4897615copy number variation1nstd200human GRCh38 chr1: 157,117,607-157,119,856 , GRCh37.p13 chr1: 157,087,399-157,089,648 ETV3
    nsv4784357copy number variation1nstd200human GRCh37 chr1: 157,087,399-157,089,649 , GRCh38.p12 chr1: 157,117,607-157,119,857 ETV3
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4534660insertion1nstd166human GRCh37.p13 chr1: 157,089,826-157,089,826 , GRCh38.p12 chr1: 157,120,034-157,120,034 ETV3
    nsv4459017mobile element insertion1nstd166human GRCh37.p13 chr1: 157,100,561-157,100,561 , GRCh38.p12 chr1: 157,130,769-157,130,769 ETV3
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
    nsv4070162copy number variation1nstd166human GRCh37.p13 chr1: 157,105,801-157,105,965 , GRCh38.p12 chr1: 157,136,009-157,136,173 ETV3
    nsv4060634copy number variation1nstd166human GRCh37.p13 chr1: 157,091,699-157,091,968 , GRCh38.p12 chr1: 157,121,907-157,122,176 ETV3
    nsv3918947copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , LOC101060227, 1608 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 , CRB1, 1608 more genes
    nsv3906950copy number variation1nstd102humanPathogenic GRCh38 chr1: 154,566,501-157,624,084 , NCBI36 chr1: 152,805,601-155,860,498 , GRCh37 chr1: 154,538,977-157,593,874 ARHGEF2-AS2, INSRR, 131 more genes
    nsv3900459copy number variation1nstd102humanPathogenic GRCh38 chr1: 149,854,269-180,267,197 , NCBI36 chr1: 148,092,455-178,502,955 , GRCh37 chr1: 149,825,831-180,236,332 HORMAD1, BCAN-AS1, 923 more genes
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