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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7053890inversion1nstd229human GRCh38 chr4: 16,156,227-18,504,313 , GRCh37.p13 chr4: 16,157,850-18,505,936 TAPT1, NCAPG, 26 more genes
    nsv7047237inversion1nstd229human GRCh38 chr4: 15,975,453-25,472,708 , GRCh37.p13 chr4: 15,977,076-25,474,330 LOC107986219, LOC102723675, 78 more genes
    nsv7044499inversion1nstd229human GRCh38 chr4: 16,435,218-18,199,516 , GRCh37.p13 chr4: 16,436,841-18,201,139 NACAP5, NCAPG, 19 more genes
    nsv6737499copy number variation1nstd229human GRCh38 chr4: 17,611,956-17,626,982 , GRCh37.p13 chr4: 17,613,579-17,628,605 MED28
    nsv6732427copy number variation1nstd229human GRCh38 chr4: 17,373,901-17,672,300 , GRCh37.p13 chr4: 17,375,524-17,673,923 MED28, NACAP5, 5 more genes
    nsv6731153copy number variation1nstd229human GRCh38 chr4: 17,627,138-17,699,944 , GRCh37.p13 chr4: 17,628,761-17,701,567 FAM184B, MED28
    nsv6728701copy number variation1nstd229human GRCh38 chr4: 17,375,401-17,812,000 , GRCh37.p13 chr4: 17,377,024-17,813,623 DCAF16, NACAP5, 7 more genes
    nsv6723184copy number variation1nstd229human GRCh38 chr4: 17,620,600-17,630,114 , GRCh37.p13 chr4: 17,622,223-17,631,737 MED28, FAM184B
    nsv6720856copy number variation1nstd229human GRCh38 chr4: 17,602,101-17,669,500 , GRCh37.p13 chr4: 17,603,724-17,671,123 LAP3, FAM184B, 1 more genes
    nsv6718330copy number variation1nstd229human GRCh38 chr4: 17,613,193-17,623,161 , GRCh37.p13 chr4: 17,614,816-17,624,784 MED28
    nsv6637075copy number variation1nstd102humanUncertain significance GRCh37 chr4: 16,249,194-24,864,955 , GRCh38.p12 chr4: 16,247,571-24,863,333 LOC107986262, QDPR, 63 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629587copy number variation1nstd224human GRCh37 chr4: 17,616,294-17,634,213 , GRCh38.p12 chr4: 17,614,671-17,632,590 FAM184B, MED28
    nsv6629211copy number variation1nstd224human GRCh37 chr4: 17,606,274-17,747,023 , GRCh38.p12 chr4: 17,604,651-17,745,400 FAM184B, LAP3, 1 more genes
    nsv6570681inversion1nstd223human GRCh38 chr4: 16,156,227-18,504,312 , GRCh37.p13 chr4: 16,157,850-18,505,935 NCAPG, LOC107986219, 26 more genes
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