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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906623copy number variation1nstd209human GRCh38 chr3: 45,938,284-45,942,636 , GRCh37.p13 chr3: 45,979,776-45,984,128 CXCR6, FYCO1
    nsv5836562copy number variation1nstd209human GRCh38 chr3: 45,938,320-45,941,919 , GRCh37.p13 chr3: 45,979,812-45,983,411 FYCO1, CXCR6
    nsv5836285copy number variation1nstd209human GRCh38 chr3: 45,984,342-45,985,341 , GRCh37.p13 chr3: 46,025,834-46,026,833 FYCO1
    nsv5836284copy number variation1nstd209human GRCh38 chr3: 45,979,842-45,981,291 , GRCh37.p13 chr3: 46,021,334-46,022,783 FYCO1
    nsv5441679copy number variation1nstd206human GRCh38 chr3: 45,924,865-45,925,180 , GRCh37.p13 chr3: 45,966,357-45,966,672 FYCO1
    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
    nsv4924387copy number variation1nstd200human GRCh38 chr3: 45,994,270-46,016,109 , GRCh37.p13 chr3: 46,035,762-46,057,601 XCR1, LOC105377063, 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
    nsv4793956copy number variation1nstd200human GRCh37 chr3: 46,035,762-46,057,601 , GRCh38.p12 chr3: 45,994,270-46,016,109 XCR1, LOC105377063, 1 more genes
    nsv4790523copy number variation1nstd200human GRCh37 chr3: 45,979,778-45,984,129 , GRCh38.p12 chr3: 45,938,286-45,942,637 CXCR6, FYCO1
    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
    nsv4588734copy number variation1nstd183human GRCh37 chr3: 45,969,433-45,977,779 , GRCh38.p12 chr3: 45,927,941-45,936,287 FYCO1
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4451167copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,862,803-46,173,511 , GRCh38.p12 chr3: 45,821,311-46,132,019 NRBF2P2, LOC105377067, 7 more genes
    nsv4407165copy number variation1nstd174human GRCh37 chr3: 46,018,826-46,018,889 , GRCh38.p12 chr3: 45,977,334-45,977,397 FYCO1
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
    nsv4091464copy number variation1nstd166human GRCh37.p13 chr3: 46,003,067-46,003,218 , GRCh38.p12 chr3: 45,961,575-45,961,726 FYCO1
    nsv3955487copy number variation1nstd168human GRCh38 chr3: 45,943,670-45,952,509 , GRCh37.p13 chr3: 45,985,162-45,994,001 CXCR6, FYCO1
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