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Items: 1 to 20 of 374

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979990inversion1nstd209human GRCh38 chr14: 105,626,484-105,858,518 , GRCh37.p13 chr14: 106,092,821-106,320,043 , ELK2AP, 19 more genes
    nsv5974559inversion1nstd209human GRCh38 chr14: 105,743,497-105,873,952 , GRCh37.p13 chr14: 106,209,834-106,320,043 IGH, IGHD, 19 more genes
    nsv5973552inversion1nstd209human GRCh38 chr14: 105,656,567-105,771,636 , GRCh37.p13 chr14: 106,122,904-106,237,973 , ELK2AP, 9 more genes
    nsv5973168inversion1nstd209human GRCh38 chr14: 105,589,366-105,862,476 , GRCh37.p13 chr14: 106,071,380-106,320,043 , ELK2AP, 25 more genes
    nsv5971606inversion1nstd209human GRCh38 chr14: 105,711,682-105,746,045 , GRCh37.p13 chr14: 106,178,019-106,212,382 , IGH, 2 more genes
    nsv5968136inversion1nstd209human GRCh38 chr14: 105,602,975-105,747,124 , GRCh37.p13 chr14: 106,071,380-106,213,461 , ELK2AP, 11 more genes
    nsv5946805copy number variation1nstd209human GRCh38 chr14: 105,710,386-105,857,349 , GRCh37.p13 chr14: 106,176,723-106,320,043 , ATP6V1G1P1, 10 more genes
    nsv5946726copy number variation1nstd209human GRCh38 chr14: 105,710,993-105,772,934 , GRCh37.p13 chr14: 106,177,330-106,239,271 , IGH, 4 more genes
    nsv5946677copy number variation1nstd209human GRCh38 chr14: 105,710,989-105,773,815 , GRCh37.p13 chr14: 106,177,326-106,240,152 , IGH, 4 more genes
    nsv5946083copy number variation1nstd209human GRCh38 chr14: 105,691,298-106,606,057 , GRCh37.p13 chr14: 106,157,635-106,929,356 , GRCh37.p13 chr14|NW_004166863.1: 516,901-1,269,224 , IGHV3-41, 148 more genes
    nsv5946021copy number variation1nstd209human GRCh38 chr14: 105,710,495-105,860,074 , GRCh37.p13 chr14: 106,176,832-106,320,043 , IGHG3, 11 more genes
    nsv5945930copy number variation1nstd209human GRCh38 chr14: 105,646,264-105,860,285 , GRCh37.p13 chr14: 106,112,601-106,320,043 , MIR4539, 16 more genes
    nsv5945737copy number variation1nstd209human GRCh38 chr14: 105,709,875-105,859,672 , GRCh37.p13 chr14: 106,176,212-106,320,043 , IGHG1, 11 more genes
    nsv5945706copy number variation1nstd209human GRCh38 chr14: 105,589,424-105,861,306 , GRCh37.p13 chr14: 106,071,380-106,320,043 , MIR4538, 22 more genes
    nsv5945662copy number variation1nstd209human GRCh38 chr14: 105,710,434-105,744,791 , GRCh37.p13 chr14: 106,176,771-106,211,128 , IGH, 2 more genes
    nsv5945638copy number variation1nstd209human GRCh38 chr14: 105,709,800-105,745,337 , GRCh37.p13 chr14: 106,176,137-106,211,674 , IGH, 2 more genes
    nsv5944880copy number variation1nstd209human GRCh38 chr14: 105,710,492-105,745,310 , GRCh37.p13 chr14: 106,176,829-106,211,647 , IGH, 2 more genes
    nsv5944807copy number variation1nstd209human GRCh38 chr14: 105,710,072-105,859,525 , GRCh37.p13 chr14: 106,176,409-106,320,043 , MIR4539, 11 more genes
    nsv5944329copy number variation1nstd209human GRCh38 chr14: 105,710,790-105,859,384 , GRCh37.p13 chr14: 106,177,127-106,320,043 , MIR4507, 11 more genes
    nsv5943848copy number variation1nstd209human GRCh38 chr14: 105,710,803-105,859,623 , GRCh37.p13 chr14: 106,177,140-106,320,043 , IGH, 11 more genes
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