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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
    nsv7042375inversion1nstd229human GRCh38 chr3: 72,118,918-72,154,609 , GRCh37.p13 chr3: 72,168,069-72,203,760 LINC00870
    nsv7041748inversion1nstd229human GRCh38 chr3: 72,070,390-75,778,215 , GRCh37.p13 chr3: 72,119,541-75,827,366 FTH1P23, LOC107986099, 66 more genes
    nsv6712385copy number variation1nstd229human GRCh38 chr3: 66,065,527-73,237,527 , GRCh37.p13 chr3: 66,051,202-73,286,678 , RNA5SP136, 79 more genes
    nsv6699199copy number variation1nstd229human GRCh38 chr3: 72,172,502-72,172,562 , GRCh37.p13 chr3: 72,221,653-72,221,713 LINC00870
    nsv6364663copy number variation1nstd223human GRCh38 chr3: 72,114,873-72,176,776 , GRCh37.p13 chr3: 72,164,024-72,225,927 LINC00870
    nsv6360720copy number variation1nstd223human GRCh38 chr3: 72,066,062-72,267,442 , GRCh37.p13 chr3: 72,115,213-72,316,593 CCDC137P1, LINC00870, 1 more genes
    nsv6360345copy number variation1nstd223human GRCh38 chr3: 72,171,128-72,172,659 , GRCh37.p13 chr3: 72,220,279-72,221,810 LINC00870
    nsv6148685copy number variation1nstd214human GRCh38 chr3: 72,172,504-72,172,561 , GRCh37.p13 chr3: 72,221,655-72,221,712 LINC00870
    nsv6134705copy number variation1nstd213human GRCh37 chr3: 66,270,000-87,730,001 , GRCh38.p12 chr3: 66,219,846-87,680,851 , AKR1B1P2, 187 more genes
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5836758copy number variation1nstd209human GRCh38 chr3: 72,174,468-72,175,817 , GRCh37.p13 chr3: 72,223,619-72,224,968 LINC00870
    nsv5564432copy number variation1nstd102humanPathogenic GRCh37 chr3: 68,939,251-72,700,418 , GRCh38.p12 chr3: 68,890,100-72,651,267 CCDC137P1, LOC105377160, 39 more genes
    nsv5435106copy number variation1nstd206human GRCh38 chr3: 72,172,502-72,172,562 , GRCh37.p13 chr3: 72,221,653-72,221,713 LINC00870
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4927332copy number variation1nstd200human GRCh38 chr3: 72,066,065-72,267,442 , GRCh37.p13 chr3: 72,115,216-72,316,593 LINC00877, LINC00870, 1 more genes
    nsv4924562copy number variation1nstd200human GRCh38 chr3: 72,022,222-72,173,160 , GRCh37.p13 chr3: 72,071,373-72,222,311 LINC00870, CCDC137P1, 1 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4728221copy number variation1nstd102humanUncertain significance GRCh37 chr3: 70,938,608-74,660,846 , GRCh38.p12 chr3: 70,889,457-74,611,695 CCDC137P1, LINC02047, 45 more genes
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