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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964488insertion1nstd209human GRCh38 chr1: 15,163,623-15,163,623 , GRCh37.p13 chr1: 15,490,119-15,490,119 TMEM51, TMEM51-AS2
    nsv5964404insertion1nstd209human GRCh38 chr1: 15,192,449-15,192,449 , GRCh37.p13 chr1: 15,518,945-15,518,945 TMEM51, MFFP1
    nsv5964349insertion1nstd209human GRCh38 chr1: 15,170,144-15,170,144 , GRCh37.p13 chr1: 15,496,640-15,496,640 TMEM51-AS2, TMEM51
    nsv5887500copy number variation1nstd209human GRCh38 chr1: 15,160,405-15,165,038 , GRCh37.p13 chr1: 15,486,901-15,491,534 TMEM51, TMEM51-AS2
    nsv5886262copy number variation1nstd209human GRCh38 chr1: 15,183,240-15,184,627 , GRCh37.p13 chr1: 15,509,736-15,511,123 TMEM51
    nsv5883799copy number variation1nstd209human GRCh38 chr1: 15,191,357-15,198,557 , GRCh37.p13 chr1: 15,517,853-15,525,053 TMEM51, MFFP1
    nsv5881621copy number variation1nstd209human GRCh38 chr1: 15,185,984-15,186,046 , GRCh37.p13 chr1: 15,512,480-15,512,542 TMEM51
    nsv5880428copy number variation1nstd209human GRCh38 chr1: 15,188,988-15,224,212 , GRCh37.p13 chr1: 15,515,484-15,550,708 TMEM51, MFFP1
    nsv5875535copy number variation1nstd209human GRCh38 chr1: 15,160,438-15,164,966 , GRCh37.p13 chr1: 15,486,934-15,491,462 TMEM51, TMEM51-AS2
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5828353copy number variation1nstd209human GRCh38 chr1: 15,183,256-15,184,599 , GRCh37.p13 chr1: 15,509,752-15,511,095 TMEM51
    nsv5828352copy number variation1nstd209human GRCh38 chr1: 15,160,580-15,164,947 , GRCh37.p13 chr1: 15,487,076-15,491,443 TMEM51-AS2, TMEM51
    nsv5828235copy number variation2nstd209human GRCh38 chr1: 15,191,134-15,198,701 , GRCh37.p13 chr1: 15,517,630-15,525,197 MFFP1, TMEM51
    nsv5828234copy number variation1nstd209human GRCh38 chr1: 15,188,630-15,223,921 , GRCh37.p13 chr1: 15,515,126-15,550,417 MFFP1, TMEM51
    nsv5688432mobile element insertion2nstd211human GRCh38 chr1: 15,163,638-15,163,638 , GRCh37.p13 chr1: 15,490,134-15,490,134 TMEM51, TMEM51-AS2
    nsv5683047mobile element insertion2nstd211human GRCh38 chr1: 15,180,236-15,180,236 , GRCh37.p13 chr1: 15,506,732-15,506,732 TMEM51
    nsv5679959mobile element insertion2nstd211human GRCh38 chr1: 15,170,160-15,170,160 , GRCh37.p13 chr1: 15,496,656-15,496,656 TMEM51-AS2, TMEM51
    nsv5621434insertion1nstd207human GRCh38 chr1: 15,163,623-15,163,623 , GRCh37.p13 chr1: 15,490,119-15,490,119 TMEM51, TMEM51-AS2
    nsv5426254copy number variation1nstd206human GRCh38 chr1: 15,187,497-15,193,921 , GRCh37.p13 chr1: 15,513,993-15,520,417 MFFP1, TMEM51
    nsv5420930copy number variation1nstd206human GRCh38 chr1: 15,160,451-15,164,967 , GRCh37.p13 chr1: 15,486,947-15,491,463 TMEM51, TMEM51-AS2
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