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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5669407inversion1nstd207human GRCh37.p13 chr3: 49,780,278-49,805,120 , GRCh38 chr3: 49,742,845-49,767,687 IP6K1, COX6CP14
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5200638copy number variation1nstd204human GRCh38.p13 chr3: 49,756,555-49,760,656 , GRCh37.p13 chr3: 49,793,988-49,798,089 IP6K1, COX6CP14
    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
    nsv4911276copy number variation1nstd200human GRCh38 chr3: 49,752,474-49,756,826 , GRCh37.p13 chr3: 49,789,907-49,794,259 COX6CP14, IP6K1
    nsv4911275copy number variation1nstd200human GRCh38 chr3: 49,750,669-49,756,702 , GRCh37.p13 chr3: 49,788,102-49,794,135 IP6K1, COX6CP14
    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
    nsv4790641copy number variation1nstd200human GRCh37 chr3: 49,788,102-49,794,135 , GRCh38.p12 chr3: 49,750,669-49,756,702 COX6CP14, IP6K1
    nsv4728146copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,807,193-51,363,558 , GRCh38.p12 chr3: 48,769,760-51,326,127 APEH, MIR5193, 90 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
    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
    nsv4091782copy number variation1nstd166human GRCh37.p13 chr3: 49,786,667-49,856,854 , GRCh38.p12 chr3: 49,749,234-49,819,421 UBA7, IP6K1, 5 more genes
    nsv4088375copy number variation1nstd166human GRCh37.p13 chr3: 49,787,013-49,809,496 , GRCh38.p12 chr3: 49,749,580-49,772,063 IP6K1, COX6CP14
    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
    nsv3912778copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,498,433-55,348,528 , GRCh38 chr3: 49,461,000-55,314,500 , NCBI36 chr3: 49,473,437-55,323,568 SEMA3G, INKA1, 160 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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