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Items: 1 to 20 of 95

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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
    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
    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
    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
    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
    nsv5836291copy number variation1nstd209human GRCh38 chr3: 47,012,184-47,016,853 , GRCh37.p13 chr3: 47,053,674-47,058,343 SETD2, NRADDP
    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
    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
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4399516copy number variation1nstd174human GRCh37 chr3: 47,016,701-47,054,700 , GRCh38.p12 chr3: 46,975,211-47,013,210 NRADDP, NBEAL2, 1 more genes
    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
    nsv3921797copy number variation1nstd102humanPathogenic NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353 RBM5-AS1, PRSS42P, 185 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
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