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Items: 1 to 20 of 273

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv7049214inversion1nstd229human GRCh38 chr1: 86,481,973-88,243,863 , GRCh37.p13 chr1: 86,947,656-88,709,546 CLCA4, CLCA3P, 25 more genes
    nsv7046575inversion1nstd229human GRCh38 chr1: 83,069,893-89,051,563 , GRCh37.p13 chr1: 83,535,576-89,517,246 LOC105378826, RN7SL583P, 87 more genes
    nsv7041208inversion1nstd229human GRCh38 chr1: 86,888,533-88,519,414 , GRCh37.p13 chr1: 87,354,216-88,985,097 RNA5SP52, LINC01364, 17 more genes
    nsv6656692copy number variation1nstd229human GRCh38 chr1: 86,908,602-86,910,660 , GRCh37.p13 chr1: 87,374,285-87,376,343 SELENOF
    nsv6656691copy number variation1nstd229human GRCh38 chr1: 86,907,537-86,907,635 , GRCh37.p13 chr1: 87,373,220-87,373,318 SELENOF
    nsv6656690copy number variation1nstd229human GRCh38 chr1: 86,903,869-86,911,927 , GRCh37.p13 chr1: 87,369,552-87,377,610 SELENOF
    nsv6656689copy number variation1nstd229human GRCh38 chr1: 86,883,404-86,883,812 , GRCh37.p13 chr1: 87,349,087-87,349,495 SELENOF
    nsv6656546copy number variation1nstd229human GRCh38 chr1: 86,854,061-86,861,409 , GRCh37.p13 chr1: 87,319,744-87,327,092 SELENOF
    nsv6656463copy number variation1nstd229human GRCh38 chr1: 86,877,801-86,883,400 , GRCh37.p13 chr1: 87,343,484-87,349,083 SELENOF
    nsv6656229copy number variation1nstd229human GRCh38 chr1: 86,893,401-86,923,700 , GRCh37.p13 chr1: 87,359,084-87,389,383 HS2ST1, SELENOF
    nsv6656227copy number variation1nstd229human GRCh38 chr1: 86,785,119-87,001,420 , GRCh37.p13 chr1: 87,250,802-87,467,103 SELENOF, RPL17P5, 2 more genes
    nsv6655671copy number variation1nstd229human GRCh38 chr1: 86,883,470-86,883,517 , GRCh37.p13 chr1: 87,349,153-87,349,200 SELENOF
    nsv6554615inversion1nstd223human GRCh38 chr1: 86,888,226-86,888,864 , GRCh37.p13 chr1: 87,353,909-87,354,547 SELENOF
    nsv6543467inversion1nstd223human GRCh38 chr1: 86,878,565-86,880,381 , GRCh37.p13 chr1: 87,344,248-87,346,064 SELENOF
    nsv6542810inversion1nstd223human GRCh38 chr1: 86,344,314-89,254,085 , GRCh37.p13 chr1: 86,809,997-89,719,768 GBP3, LOC105378838, 52 more genes
    nsv6542421inversion1nstd223human GRCh38 chr1: 85,951,963-92,104,665 , GRCh37.p13 chr1: 86,417,646-92,570,222 LOC105378844, LINC01773, 104 more genes
    nsv6538710inversion1nstd223human GRCh38 chr1: 86,872,420-86,873,062 , GRCh37.p13 chr1: 87,338,103-87,338,745 SELENOF
    nsv6536739inversion1nstd223human GRCh38 chr1: 86,344,291-89,254,074 , GRCh37.p13 chr1: 86,809,974-89,719,757 LOC105378835, RPL7L1P22, 52 more genes
    nsv6321695copy number variation1nstd223human GRCh38 chr1: 86,896,901-86,925,400 , GRCh37.p13 chr1: 87,362,584-87,391,083 SELENOF, HS2ST1
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