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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7098849copy number variation1nstd102humanPathogenic GRCh37 chr3: 110,943,783-115,859,912 , GRCh38.p12 chr3: 111,224,936-116,141,065 ATG3, SIDT1, 81 more genes
    nsv7096436copy number variation1nstd102humanUncertain significance GRCh37 chr3: 113,503,051-114,070,745 , GRCh38.p12 chr3: 113,784,204-114,351,898 ZNF80, H2BP3, 16 more genes
    nsv7096435copy number variation1nstd102humanUncertain significance GRCh37 chr3: 113,010,404-114,099,634 , GRCh38.p12 chr3: 113,291,557-114,380,787 USF3, VPS26AP1, 27 more genes
    nsv7051524inversion1nstd229human GRCh38 chr3: 110,492,556-118,654,181 , GRCh37.p13 chr3: 110,211,403-118,373,028 MIR8076, ZBTB20-AS4, 106 more genes
    nsv6707907copy number variation1nstd229human GRCh38 chr3: 113,856,250-122,791,940 , GRCh37.p13 chr3: 113,575,097-122,510,787 COX17, LOC105374052, 133 more genes
    nsv6705447copy number variation1nstd229human GRCh38 chr3: 114,083,902-114,092,875 , GRCh37.p13 chr3: 113,802,749-113,811,722 QTRT2
    nsv6703331copy number variation1nstd229human GRCh38 chr3: 114,067,659-114,151,963 , GRCh37.p13 chr3: 113,786,506-113,870,810 QTRT2, DRD3, 1 more genes
    nsv6701093copy number variation1nstd229human GRCh38 chr3: 114,043,920-114,060,946 , GRCh37.p13 chr3: 113,762,767-113,779,793 CCDC191, QTRT2
    nsv6698226copy number variation1nstd229human GRCh38 chr3: 114,076,430-114,091,975 , GRCh37.p13 chr3: 113,795,277-113,810,822 QTRT2
    nsv6636830copy number variation1nstd102humanPathogenic GRCh37 chr3: 107,059,705-115,005,256 , GRCh38.p12 chr3: 107,340,858-115,286,409 ATP6V1A, DRD3, 117 more genes
    nsv6369996copy number variation1nstd223human GRCh38 chr3: 114,076,430-114,091,942 , GRCh37.p13 chr3: 113,795,277-113,810,789 QTRT2
    nsv6315408copy number variation1nstd102humanPathogenic GRCh37 chr3: 106,598,767-115,704,696 , GRCh38.p12 chr3: 106,879,920-115,985,849 DZIP3, MIR9900, 138 more genes
    nsv6254542mobile element insertion1nstd215human GRCh38 chr3: 114,071,748-114,071,748 , GRCh37.p13 chr3: 113,790,595-113,790,595 QTRT2
    nsv6134776copy number variation1nstd213human GRCh37 chr3: 105,120,000-116,510,001 , GRCh38.p12 chr3: 105,401,156-116,791,154 , ALCAM, 156 more genes
    nsv6134388copy number variation1nstd213human GRCh37 chr3: 113,520,000-114,250,001 , GRCh38.p12 chr3: 113,801,153-114,531,154 ATP6V1A, DRD3, 17 more genes
    nsv5675029mobile element insertion1nstd211human GRCh38 chr3: 114,078,898-114,078,898 , GRCh37.p13 chr3: 113,797,745-113,797,745 QTRT2
    nsv5674224copy number variation1nstd102humanPathogenic GRCh37 chr3: 113,623,035-114,368,128 , GRCh38.p12 chr3: 113,904,188-114,649,281 VPS26AP1, ATOSBP1, 14 more genes
    nsv5544925insertion1nstd206human GRCh38 chr3: 114,084,242-114,084,280 , GRCh37.p13 chr3: 113,803,089-113,803,127 QTRT2
    nsv5449261copy number variation1nstd206human GRCh38 chr3: 114,072,707-114,074,007 , GRCh37.p13 chr3: 113,791,554-113,792,854 QTRT2
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