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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5327857inversion1nstd204human GRCh37.p13 chr10: 115,288,018-116,786,304 , GRCh38.p13 chr10: 113,528,259-115,723,405 , ADRB1, 31 more genes
    nsv5029881inversion1nstd200human GRCh38 chr10: 113,528,269-115,723,396 , GRCh37.p13 chr10: 115,288,028-116,786,295 , NHLRC2, 31 more genes
    nsv4880587inversion1nstd200human GRCh37 chr10: 115,288,028-117,482,906 , GRCh38.p12 chr10: 113,528,269-115,723,396 , NHLRC2, 31 more genes
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
    nsv4455202copy number variation1nstd102humanUncertain significance GRCh37 chr10: 116,139,681-116,522,804 , GRCh38.p12 chr10: 114,379,922-114,763,045 AFAP1L2, ABLIM1, 3 more genes
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 more genes
    nsv4183720copy number variation1nstd166human GRCh37.p13 chr10: 116,030,341-117,443,667 , GRCh38.p12 chr10: 114,270,582-115,684,157 VWA2, AFAP1L2, 14 more genes
    nsv3938579copy number variation1nstd167human GRCh37 chr10: 116,529,174-116,529,214 , GRCh38.p12 chr10: 114,769,415-114,769,455 ABLIM1, LOC101927692
    nsv3923859copy number variation1nstd102humanPathogenic NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674 AS-PTPRE, SFXN4, 330 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 more genes
    nsv3923247copy number variation1nstd102humanLikely benign NCBI36 chr10: 116,334,631-116,846,342 , GRCh38 chr10: 114,584,882-115,096,595 , GRCh37 chr10: 116,344,641-116,856,352 RPL15P13, FHIP2A, 10 more genes
    nsv3923141copy number variation1nstd102humanPathogenic NCBI36 chr10: 116,334,631-118,765,408 , GRCh38 chr10: 114,584,882-117,015,907 , GRCh37 chr10: 116,344,641-118,775,418 SPMIP5, LINC02626, 32 more genes
    nsv3922500copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 112,554,483-116,633,759 , GRCh37 chr10: 112,564,493-116,643,769 , GRCh38 chr10: 110,804,735-114,884,010 ADRA2A, ADRB1, 57 more genes
    nsv3922274copy number variation1nstd102humanUncertain significance NCBI36 chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422 DPCD, LOC105378467, 504 more genes
    nsv3921919copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082 MIR4295, BORCS7, 508 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3919820copy number variation1nstd102humanPathogenic GRCh38 chr10: 107,191,100-118,761,489 , GRCh37 chr10: 108,950,858-120,521,001 , NCBI36 chr10: 108,940,848-120,510,991 CCDC186, RN7SKP288, 147 more genes
    nsv3915987copy number variation1nstd102humanPathogenic GRCh38 chr10: 112,074,094-115,537,174 , GRCh37 chr10: 113,833,852-117,032,437 , NCBI36 chr10: 113,823,842-117,286,674 LOC103344931, LINC02626, 48 more genes
    nsv3914619copy number variation1nstd102humanPathogenic NCBI36 chr10: 111,418,518-126,431,209 , GRCh37.p13 chr10: 111,428,528-126,441,219 , GRCh38.p12 chr10: 109,668,770-124,752,650 LOC103344931, LINC02626, 225 more genes
    nsv3912079copy number variation1nstd102humanPathogenic NCBI36 chr10: 109,852,335-135,284,168 , GRCh38 chr10: 108,102,587-133,620,674 , GRCh37 chr10: 109,862,345-135,434,178 TUBGCP2, SHOC2, 372 more genes
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