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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv6713643copy number variation1nstd229human GRCh38 chr3: 45,872,276-45,886,741 , GRCh37.p13 chr3: 45,913,768-45,928,233 CCR9, LZTFL1, 1 more genes
    nsv6713263copy number variation1nstd229human GRCh38 chr3: 45,891,832-45,892,698 , GRCh37.p13 chr3: 45,933,324-45,934,190 CCR9, LZTFL1
    nsv6706205copy number variation1nstd229human GRCh38 chr3: 45,885,326-45,890,315 , GRCh37.p13 chr3: 45,926,818-45,931,807 CCR9, LZTFL1
    nsv6700096copy number variation1nstd229human GRCh38 chr3: 45,890,856-45,922,713 , GRCh37.p13 chr3: 45,932,348-45,964,205 CCR9, LZTFL1, 1 more genes
    nsv6700069copy number variation1nstd229human GRCh38 chr3: 45,896,362-46,914,422 , GRCh37.p13 chr3: 45,937,854-46,955,912 LINC02009, ALS2CL, 32 more genes
    nsv6365945copy number variation1nstd223human GRCh38 chr3: 45,897,016-45,897,643 , GRCh37.p13 chr3: 45,938,508-45,939,135 LZTFL1, CCR9
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6076022insertion1nstd212human GRCh38 chr3: 45,890,269-45,890,269 , GRCh37.p13 chr3: 45,931,761-45,931,761 LZTFL1, CCR9
    nsv5964356insertion1nstd209human GRCh38 chr3: 45,890,270-45,890,270 , GRCh37.p13 chr3: 45,931,762-45,931,762 CCR9, LZTFL1
    nsv5619364insertion2nstd207human GRCh38 chr3: 45,890,269-45,890,269 , GRCh37.p13 chr3: 45,931,761-45,931,761 LZTFL1, CCR9
    nsv5609633insertion1nstd207human GRCh38 chr3: 45,890,308-45,890,308 , GRCh37.p13 chr3: 45,931,800-45,931,800 CCR9, LZTFL1
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 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
    nsv4754518insertion1nstd199human GRCh37 chr3: 45,931,761-45,931,761 , GRCh38.p12 chr3: 45,890,269-45,890,269 CCR9, LZTFL1
    nsv4683137copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,867,806-46,063,439 , GRCh38.p12 chr3: 45,826,314-46,021,947 CXCR6, SDHDP4, 6 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4470958mobile element insertion1nstd166human GRCh37.p13 chr3: 45,934,017-45,934,017 , GRCh38.p12 chr3: 45,892,525-45,892,525 CCR9, LZTFL1
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