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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140723copy number variation1nstd232human GRCh37.p13 chr3: 47,019,993-47,020,111 , GRCh38.p12 chr3: 46,978,503-46,978,621 NBEAL2, CCDC12
    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
    nsv6714023copy number variation1nstd229human GRCh38 chr3: 46,936,048-47,025,302 , GRCh37.p13 chr3: 46,977,538-47,066,792 CCDC12, NRADDP, 2 more genes
    nsv6713511copy number variation1nstd229human GRCh38 chr3: 46,395,301-47,630,000 , GRCh37.p13 chr3: 46,436,792-47,671,490 BOLA2P2, LRRC2-AS1, 36 more genes
    nsv6712869copy number variation1nstd229human GRCh38 chr3: 46,996,893-46,999,313 , GRCh37.p13 chr3: 47,038,383-47,040,803 NBEAL2
    nsv6712784copy number variation1nstd229human GRCh38 chr3: 46,980,370-46,980,583 , GRCh37.p13 chr3: 47,021,860-47,022,073 NBEAL2, CCDC12
    nsv6703235copy number variation1nstd229human GRCh38 chr3: 46,998,199-47,006,654 , GRCh37.p13 chr3: 47,039,689-47,048,144 NBEAL2
    nsv6364035copy number variation1nstd223human GRCh38 chr3: 46,977,446-46,981,361 , GRCh37.p13 chr3: 47,018,936-47,022,851 NBEAL2, CCDC12
    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
    nsv6297721copy number variation1nstd186human GRCh37 chr3: 46,977,878-47,173,020 , GRCh38.p12 chr3: 46,936,388-47,131,530 NBEAL2, SETD2, 3 more genes
    nsv6253965mobile element insertion1nstd215human GRCh38 chr3: 47,007,820-47,007,820 , GRCh37.p13 chr3: 47,049,310-47,049,310 NBEAL2
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5898717copy number variation1nstd209human GRCh38 chr3: 46,977,254-46,981,314 , GRCh37.p13 chr3: 47,018,744-47,022,804 NBEAL2, CCDC12
    nsv5888582copy number variation1nstd209human GRCh38 chr3: 46,802,705-48,210,414 , GRCh37.p13 chr3: 46,844,195-48,251,904 SNORD13P3, LOC105377074, 34 more genes
    nsv5836290copy number variation1nstd209human GRCh38 chr3: 46,977,052-46,981,047 , GRCh37.p13 chr3: 47,018,542-47,022,537 NBEAL2, CCDC12
    nsv5836007copy number variation1nstd209human GRCh38 chr3: 46,986,607-46,995,060 , GRCh37.p13 chr3: 47,028,097-47,036,550 NBEAL2
    nsv5835991copy number variation1nstd209human GRCh38 chr3: 47,008,434-47,009,783 , GRCh37.p13 chr3: 47,049,924-47,051,273 NRADDP, NBEAL2
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5453738copy number variation1nstd206human GRCh38 chr3: 46,936,388-47,131,530 , GRCh37.p13 chr3: 46,977,878-47,173,020 MRPL57P3, NBEAL2, 3 more genes
    nsv5351739translocation1nstd200human GRCh38 chr3: 46,978,515-46,978,515 , GRCh38 chr3: 46,978,622-46,978,622 , GRCh37.p13 chr3: 47,020,112-47,020,112 , GRCh37.p13 chr3: 47,020,005-47,020,005 NBEAL2, CCDC12
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