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Items: 1 to 20 of 513

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147465copy number variation1nstd232human GRCh37.p13 chrX: 109,932,706-109,932,765 , GRCh38.p12 chrX: 110,689,478-110,689,537 CHRDL1
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098491copy number variation1nstd102humanPathogenic GRCh37 chrX: 110,005,903-110,006,055 , GRCh38.p12 chrX: 110,762,675-110,762,827 CHRDL1
    nsv7098214copy number variation1nstd102humanUncertain significance GRCh37 chrX: 109,919,459-111,003,227 , GRCh38.p12 chrX: 110,676,231-111,759,999 RNU6-496P, FCF1P4, 11 more genes
    nsv7082349copy number variation1nstd229human GRCh38 chrX: 110,789,263-110,789,331 , GRCh37.p13 chrX: 110,032,491-110,032,559 CHRDL1
    nsv7082348copy number variation1nstd229human GRCh38 chrX: 110,783,595-110,783,843 , GRCh37.p13 chrX: 110,026,823-110,027,071 CHRDL1
    nsv7082347copy number variation1nstd229human GRCh38 chrX: 110,774,701-110,780,700 , GRCh37.p13 chrX: 110,017,929-110,023,928 CHRDL1
    nsv7082346copy number variation1nstd229human GRCh38 chrX: 110,698,162-110,698,787 , GRCh37.p13 chrX: 109,941,390-109,942,015 CHRDL1
    nsv7082345copy number variation1nstd229human GRCh38 chrX: 110,696,526-110,697,306 , GRCh37.p13 chrX: 109,939,754-109,940,534 CHRDL1
    nsv7082344copy number variation1nstd229human GRCh38 chrX: 110,695,401-110,697,900 , GRCh37.p13 chrX: 109,938,629-109,941,128 CHRDL1
    nsv7082343copy number variation1nstd229human GRCh38 chrX: 110,695,374-110,698,913 , GRCh37.p13 chrX: 109,938,602-109,942,141 CHRDL1
    nsv7082342copy number variation1nstd229human GRCh38 chrX: 110,694,701-110,697,000 , GRCh37.p13 chrX: 109,937,929-109,940,228 CHRDL1
    nsv7082341copy number variation1nstd229human GRCh38 chrX: 110,694,101-110,698,900 , GRCh37.p13 chrX: 109,937,329-109,942,128 CHRDL1
    nsv7082340copy number variation1nstd229human GRCh38 chrX: 110,689,001-110,698,900 , GRCh37.p13 chrX: 109,932,229-109,942,128 CHRDL1
    nsv7082339copy number variation1nstd229human GRCh38 chrX: 110,688,901-110,698,900 , GRCh37.p13 chrX: 109,932,129-109,942,128 CHRDL1
    nsv7082338copy number variation1nstd229human GRCh38 chrX: 110,683,223-110,683,256 , GRCh37.p13 chrX: 109,926,451-109,926,484 CHRDL1
    nsv7082337copy number variation1nstd229human GRCh38 chrX: 110,680,580-110,698,531 , GRCh37.p13 chrX: 109,923,808-109,941,759 CHRDL1
    nsv7082309copy number variation1nstd229human GRCh38 chrX: 110,291,366-110,685,524 , GRCh37.p13 chrX: 109,534,594-109,928,752 RTL9, GNG5B, 5 more genes
    nsv7050030inversion1nstd229human GRCh38 chrX: 110,529,712-111,078,753 , GRCh37.p13 chrX: 109,772,940-110,321,981 PAK3, CHRDL1, 1 more genes
    nsv7047383inversion1nstd229human GRCh38 chrX: 110,759,391-110,759,452 , GRCh37.p13 chrX: 110,002,619-110,002,680 CHRDL1
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