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Items: 1 to 20 of 347

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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
    nsv7057425inversion1nstd229human GRCh38 chr4: 3,715,710-4,814,110 , GRCh37.p13 chr4: 3,717,437-4,815,837 UNC93B4, STX18, 30 more genes
    nsv6736166copy number variation1nstd229human GRCh38 chr4: 3,268,098-4,744,559 , GRCh37.p13 chr4: 3,269,825-4,746,286 LOC105374355, LOC105374358, 40 more genes
    nsv6725447copy number variation1nstd229human GRCh38 chr4: 3,485,667-4,651,685 , GRCh37.p13 chr4: 3,487,394-4,653,412 LOC101928217, LRPAP1, 34 more genes
    nsv6725356copy number variation1nstd229human GRCh38 chr4: 3,615,597-4,391,332 , GRCh37.p13 chr4: 3,617,324-4,393,059 ADRA2C, OR7E43P, 25 more genes
    nsv6636582copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359 NELFA, OR7E111FP, 289 more genes
    nsv6636256copy number variation1nstd102humanPathogenic GRCh37 chr4: 1-12,785,001 , GRCh38.p12 chr4: 10,001-12,783,377 AFAP1-AS1, LOC389199, 294 more genes
    nsv6635100copy number variation1nstd227human GRCh38.p12 chr4: 3,753,091-3,864,430 , GRCh37 chr4: 3,754,818-3,866,157 ADRA2C, LINC02600
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629440copy number variation1nstd224human GRCh37 chr4: 3,702,481-3,874,052 , GRCh38.p12 chr4: 3,700,754-3,872,325 LINC02600, ADRA2C
    nsv6366311copy number variation1nstd223human GRCh38 chr4: 3,426,615-4,165,741 , GRCh37.p13 chr4: 3,428,342-4,167,468 LOC105374358, FAM86EP, 24 more genes
    nsv6356242copy number variation1nstd223human GRCh38 chr4: 3,501,969-3,910,278 , GRCh37.p13 chr4: 3,503,696-3,912,005 LRPAP1, LINC02600, 8 more genes
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
    nsv6315365copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-5,579,467 , GRCh38.p12 chr4: 68,453-5,577,740 LOC107986246, FAM53A, 149 more genes
    nsv6315347copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952 LOC100421802, ADRA2C, 375 more genes
    nsv6314815copy number variation1nstd102humanLikely pathogenic GRCh38 chr4: 3,083,700-7,589,946 , GRCh37.p13 chr4: 3,085,427-7,591,673 ADRA2C, CRMP1, 91 more genes
    nsv6291097copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,587,167 , GRCh38.p12 chr4: 68,453-20,585,544 LOC105374479, LOC105374502, 372 more genes
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