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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
    nsv5971929inversion1nstd209human GRCh38 chr7: 117,371,293-117,373,262 , GRCh37.p13 chr7: 117,011,347-117,013,316 ASZ1
    nsv5865185copy number variation1nstd209human GRCh38 chr7: 117,369,763-117,370,908 , GRCh37.p13 chr7: 117,009,817-117,010,962 ASZ1
    nsv5861097copy number variation2nstd209human GRCh38 chr7: 117,380,245-117,381,444 , GRCh37.p13 chr7: 117,020,299-117,021,498 ASZ1
    nsv5684359mobile element insertion1nstd211human GRCh38 chr7: 117,416,535-117,416,535 , GRCh37.p13 chr7: 117,056,589-117,056,589 ASZ1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5556248sequence alteration1nstd206human GRCh38 chr7: 117,371,091-117,373,263 , GRCh37.p13 chr7: 117,011,145-117,013,317 ASZ1
    nsv5545841insertion1nstd206human GRCh38 chr7: 117,373,257-117,373,257 , GRCh37.p13 chr7: 117,013,311-117,013,311 ASZ1
    nsv5483446copy number variation1nstd206human GRCh38 chr7: 117,422,669-117,430,004 , GRCh37.p13 chr7: 117,062,723-117,070,058 ASZ1
    nsv5480923copy number variation1nstd206human GRCh38 chr7: 117,375,407-117,379,154 , GRCh37.p13 chr7: 117,015,461-117,019,208 ASZ1
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 TMEM229A, ST7-OT3, 110 more genes
    nsv5381393copy number variation1nstd102humanUncertain significance GRCh37 chr7: 116,339,139-117,307,162 , GRCh38.p12 chr7: 116,699,085-117,667,108 LOC105375466, MIR6132, 21 more genes
    nsv5371064translocation1nstd200human GRCh38 chr7: 117,417,415-117,417,415 , GRCh38 chr7: 117,420,738-117,420,738 , GRCh37.p13 chr7: 117,057,469-117,057,469 , GRCh37.p13 chr7: 117,060,792-117,060,792 ASZ1
    nsv5371063translocation1nstd200human GRCh38 chr7: 117,410,506-117,410,506 , GRCh38 chr7: 117,421,286-117,421,286 , GRCh37.p13 chr7: 117,050,560-117,050,560 , GRCh37.p13 chr7: 117,061,340-117,061,340 ASZ1
    nsv5371062translocation1nstd200human GRCh38 chr7: 117,394,363-117,394,363 , GRCh38 chr7: 117,398,094-117,398,094 , GRCh37.p13 chr7: 117,038,148-117,038,148 , GRCh37.p13 chr7: 117,034,417-117,034,417 ASZ1
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5253564copy number variation1nstd204human GRCh38.p13 chr7: 117,373,701-117,384,600 , GRCh37.p13 chr7: 117,013,755-117,024,654 ASZ1
    nsv5240787copy number variation1nstd204human GRCh38.p13 chr7: 117,408,201-117,413,800 , GRCh37.p13 chr7: 117,048,255-117,053,854 ASZ1
    nsv5181381mobile element insertion1nstd203human GRCh38 chr7: 117,375,505-117,375,521 , GRCh37.p13 chr7: 117,015,559-117,015,575 ASZ1
    nsv5119931mobile element insertion1nstd203human GRCh38 chr7: 117,408,527-117,408,539 , GRCh37.p13 chr7: 117,048,581-117,048,593 ASZ1
    nsv5112043mobile element insertion1nstd203human GRCh38 chr7: 117,366,549-117,366,551 , GRCh37.p13 chr7: 117,006,603-117,006,605 ASZ1
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