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Items: 1 to 20 of 522

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148054copy number variation1nstd102humanPathogenic GRCh37 chr1: 142,535,935-157,648,813 , GRCh38.p12 chr1: 120,175,847-149,601,750 , TRN-GTT12-1, 266 more genes
    nsv7148051copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,474,687-147,415,708 , GRCh38.p12 chr1: 147,003,128-147,943,594 LOC728989, RNU1-151P, 27 more genes
    nsv7137086copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,465,878-147,416,212 , GRCh38.p12 chr1: 146,994,332-147,944,098 SSBL4P, OR13Z2P, 28 more genes
    nsv7098839copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,405,854-147,597,284 , GRCh38.p12 chr1: 145,598,009-149,077,123 CCT8P1, LINC01719, 120 more genes
    nsv7098724copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,397,357-148,344,744 , GRCh38.p12 chr1: 144,536,526-148,549,211 , LOC105371217, 150 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7046584inversion1nstd229human GRCh38 chr1: 147,917,268-148,010,672 , GRCh37.p13 chr1|NW_003871055.3: 4,732,681-4,826,085 TRR-CCT6-2, GPR89B, 2 more genes
    nsv7041638inversion1nstd229human GRCh38 chr1: 147,918,170-148,370,143 , GRCh37.p13 chr1|NW_003871055.3: 4,733,583-5,185,556 TRE-TTC6-1, TRQ-CTG9-1, 27 more genes
    nsv7039350inversion1nstd229human GRCh38 chr1: 147,984,538-148,011,956 , GRCh37.p13 chr1|NW_003871055.3: 4,799,951-4,827,369 GPR89B, TRR-CCT6-2, 1 more genes
    nsv6641881copy number variation1nstd229human GRCh38 chr1: 147,961,601-147,983,700 , GRCh37.p13 chr1|NW_003871055.3: 4,777,014-4,799,113 GPR89B
    nsv6641880copy number variation1nstd229human GRCh38 chr1: 147,920,401-147,926,400 , GRCh37.p13 chr1: 147,392,529-147,398,513 , GRCh37.p13 chr1|NW_003871055.3: 4,735,814-4,741,813 LOC105371229, GPR89B
    nsv6641878copy number variation1nstd229human GRCh38 chr1: 147,904,678-147,985,714 , GRCh37.p13 chr1|NW_003871055.3: 4,720,091-4,801,127 , GRCh37.p13 chr1: 147,376,805-147,457,946 GJA8, LOC105371229, 1 more genes
    nsv6636744copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,493,131-147,831,043 , GRCh38.p12 chr1: 145,430,980-148,358,916 PDZK1, ANKRD34A, 102 more genes
    nsv6634386copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,626,685-147,597,284 , GRCh38.p12 chr1: 145,430,980-148,125,001 LOC391092, NBPF10, 84 more genes
    nsv6634349copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,157,447-148,016,122 , GRCh38.p12 chr1: 144,536,526-149,492,442 , TRN-GTT10-1, 170 more genes
    nsv6545815inversion1nstd223human GRCh38 chr1: 146,946,539-148,140,447 , GRCh37.p13 chr1|NW_003871055.3: 3,761,952-4,955,860 , LOC391092, 39 more genes
    nsv6542731inversion1nstd223human GRCh38 chr1: 147,056,374-148,969,054 , GRCh37.p13 chr1|NW_003871055.3: 3,871,787-5,784,467 , LINC01731, 75 more genes
    nsv6333880copy number variation1nstd223human GRCh38 chr1: 145,488,103-148,061,210 , GRCh37.p13 chr1|NW_003871055.3: 2,303,516-4,876,623 , TRR-CCT6-2, 79 more genes
    nsv6328105copy number variation1nstd223human GRCh38 chr1: 147,957,501-147,958,900 , GRCh37.p13 chr1|NW_003871055.3: 4,772,914-4,774,313 GPR89B
    nsv6327819copy number variation1nstd223human GRCh38 chr1: 147,372,943-148,292,223 , GRCh37.p13 chr1|NW_003871055.3: 4,188,356-5,107,636 , PFN1P4, 33 more genes
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