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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7077542inversion1nstd229human GRCh38 chr12: 7,565,102-9,354,075 , GRCh37.p13 chr12: 7,717,698-9,506,671 ALG1L10P, RPL15P17, 69 more genes
    nsv7076814inversion1nstd229human GRCh38 chr12: 9,221,714-9,270,499 , GRCh37.p13 chr12: 9,374,310-9,423,095 A2MP1, PTMAP4, 2 more genes
    nsv7074732inversion1nstd229human GRCh38 chr12: 9,199,258-9,594,738 , GRCh37.p13 chr12: 9,351,854-9,747,334 KLRB1, PZP, 14 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068010inversion1nstd229human GRCh38 chr12: 7,025,778-10,225,656 , GRCh37.p13 chr12: 7,178,850-10,378,255 GOT2P3, CLEC2B, 123 more genes
    nsv7065364inversion1nstd229human GRCh38 chr12: 9,198,710-9,372,424 , GRCh37.p13 chr12: 9,351,306-9,525,020 PZP, PTMAP4, 8 more genes
    nsv7064008inversion1nstd229human GRCh38 chr12: 6,716,253-10,225,825 , GRCh37.p13 chr12: 6,825,419-10,378,424 PTMAP4, COPS7A, 153 more genes
    nsv7059773inversion1nstd229human GRCh38 chr12: 8,963,554-9,585,969 , GRCh37.p13 chr12: 9,116,150-9,738,565 DDX12P, LOC105369647, 20 more genes
    nsv6637627copy number variation1nstd102humanUncertain significance GRCh37 chr12: 8,781,515-9,605,163 , GRCh38.p12 chr12: 8,628,919-9,452,567 A2MP1, LOC101928030, 26 more genes
    nsv6637226copy number variation1nstd102humanUncertain significance GRCh37 chr12: 9,358,484-9,613,948 , GRCh38.p12 chr12: 9,205,888-9,461,352 LOC728715, LINC02367, 11 more genes
    nsv6240647mobile element insertion1nstd215human GRCh38 chr12: 9,230,270-9,230,270 , GRCh37.p13 chr12: 9,382,866-9,382,866 A2MP1
    nsv6132720copy number variation1nstd213human GRCh37 chr12: 9,040,000-17,930,001 , GRCh38.p12 chr12: 8,887,404-17,777,067 A2M, A2MP1, 215 more genes
    nsv6132621copy number variation1nstd213human GRCh37 chr12: 9,330,000-9,630,001 , GRCh38.p12 chr12: 9,177,404-9,477,405 KLRG1, LOC642846, 11 more genes
    nsv6132616copy number variation1nstd213human GRCh37 chr12: 8,100,000-12,900,001 , GRCh38.p12 chr12: 7,947,404-12,747,067 A2M, A2MP1, 178 more genes
    nsv6132518copy number variation1nstd213human GRCh37 chr12: 9,010,000-10,480,001 , GRCh38.p12 chr12: 8,857,404-10,327,402 CD69, CLEC1A, 56 more genes
    nsv6132445copy number variation1nstd213human GRCh37 chr12: 9,040,000-11,190,001 , GRCh38.p12 chr12: 8,887,404-11,037,402 A2M, A2MP1, 95 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6108976inversion1nstd212human GRCh38 chr12: 9,199,258-9,594,739 , GRCh37.p13 chr12: 9,351,854-9,747,335 , A2MP1, 16 more genes
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
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