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Items: 1 to 20 of 195

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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
    nsv7045832inversion1nstd229human GRCh38 chr3: 45,971,930-45,979,972 , GRCh37.p13 chr3: 46,013,422-46,021,464 FYCO1
    nsv6713889copy number variation1nstd229human GRCh38 chr3: 45,993,873-45,997,496 , GRCh37.p13 chr3: 46,035,365-46,038,988 FYCO1, LOC105377063
    nsv6713882copy number variation1nstd229human GRCh38 chr3: 45,993,113-45,995,344 , GRCh37.p13 chr3: 46,034,605-46,036,836 LOC105377063, FYCO1
    nsv6709830copy number variation1nstd229human GRCh38 chr3: 45,967,556-45,967,727 , GRCh37.p13 chr3: 46,009,048-46,009,219 FYCO1
    nsv6708637copy number variation1nstd229human GRCh38 chr3: 45,926,301-45,929,300 , GRCh37.p13 chr3: 45,967,793-45,970,792 FYCO1
    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
    nsv6700046copy number variation1nstd229human GRCh38 chr3: 45,938,286-45,942,640 , GRCh37.p13 chr3: 45,979,778-45,984,132 FYCO1, CXCR6
    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
    nsv6253959mobile element insertion1nstd215human GRCh38 chr3: 45,966,448-45,966,448 , GRCh37.p13 chr3: 46,007,940-46,007,940 FYCO1
    nsv6154281copy number variation1nstd214human GRCh38 chr3: 45,916,488-45,916,538 , GRCh37.p13 chr3: 45,957,980-45,958,030 LZTFL1, FYCO1
    nsv6062023insertion1nstd212human GRCh38 chr3: 45,925,092-45,925,092 , GRCh37.p13 chr3: 45,966,584-45,966,584 FYCO1
    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
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