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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5418683copy number variation1nstd206human GRCh38 chr1: 166,854,955-166,855,019 , GRCh37.p13 chr1: 166,824,192-166,824,256 POGK, TADA1
    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
    nsv5041452inversion1nstd200human GRCh38 chr1: 163,441,139-169,028,376 , GRCh37.p13 chr1: 163,410,929-168,997,614 , RPS17P6, 97 more genes
    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
    nsv4728711copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 164,608,682-169,216,098 , GRCh38.p12 chr1: 164,639,445-169,246,860 ALDH9A1, ATP1B1, 95 more genes
    nsv4674180copy number variation1nstd102humanUncertain significance GRCh37 chr1: 166,284,108-167,681,975 , GRCh38.p12 chr1: 166,314,871-167,712,738 CNN2P10, LINC01363, 28 more genes
    nsv4536524insertion1nstd166human GRCh37.p13 chr1: 166,824,192-166,824,192 , GRCh38.p12 chr1: 166,854,955-166,854,955 TADA1, POGK
    nsv4518410copy number variation1nstd166human GRCh37.p13 chr1: 166,824,192-166,824,256 , GRCh38.p12 chr1: 166,854,955-166,855,019 TADA1, POGK
    nsv4453493copy number variation1nstd102humanPathogenic GRCh37 chr1: 163,093,021-168,991,239 , GRCh38.p12 chr1: 163,123,231-169,022,001 RNU6-755P, GCSHP5, 101 more genes
    nsv4453052copy number variation1nstd102humanUncertain significance GRCh37 chr1: 165,989,619-166,951,388 , GRCh38.p12 chr1: 166,020,382-166,982,151 RNA5SP64, RPL4P2, 18 more genes
    nsv4450412copy number variation1nstd102humanPathogenic GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186 FCGR3B, SLAMF9, 302 more genes
    nsv4346684copy number variation1nstd102humanPathogenic GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189 LINC00626, RN7SL861P, 359 more genes
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
    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
    nsv3906717copy number variation1nstd102humanPathogenic GRCh38 chr1: 159,479,887-166,895,086 , GRCh37 chr1: 159,449,677-166,864,323 , NCBI36 chr1: 157,716,301-165,130,947 NOS1AP, LY9, 220 more genes
    nsv3904950copy number variation1nstd102humanPathogenic GRCh38 chr1: 166,762,832-175,327,423 , NCBI36 chr1: 164,998,693-173,563,182 , GRCh37 chr1: 166,732,069-175,296,559 LINC01681, SELE, 186 more genes
    nsv3902929copy number variation1nstd102humanUncertain significance GRCh38 chr1: 166,031,546-166,979,276 , GRCh37 chr1: 166,000,783-166,948,513 , NCBI36 chr1: 164,267,407-165,215,137 MAEL, DUTP6, 17 more genes
    nsv3901593copy number variation1nstd102humanPathogenic NCBI36 chr1: 161,618,937-174,112,781 , GRCh37 chr1: 163,352,313-175,846,158 , GRCh38 chr1: 163,382,523-175,877,022 NME7, LOC105371618, 233 more genes
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