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Items: 1 to 20 of 495

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071931inversion1nstd229human GRCh38 chr12: 55,156,710-64,781,897 , GRCh37.p13 chr12: 55,550,494-65,175,677 ZBTB39, MIR548Z, 236 more genes
    nsv7069614inversion1nstd229human GRCh38 chr12: 57,953,160-64,335,038 , GRCh37.p13 chr12: 58,346,943-64,728,818 LOC100419700, LOC105369793, 67 more genes
    nsv7069192inversion1nstd229human GRCh38 chr12: 60,220,562-64,985,387 , GRCh37.p13 chr12: 60,614,343-65,379,167 KLF17P1, DPY19L2, 60 more genes
    nsv7066910inversion1nstd229human GRCh38 chr12: 60,203,453-65,465,649 , GRCh37.p13 chr12: 60,597,234-65,859,429 RPS11P6, MSRB3-AS1, 68 more genes
    nsv7064501inversion1nstd229human GRCh38 chr12: 60,432,939-65,464,484 , GRCh37.p13 chr12: 60,826,720-65,858,264 RSL24D1P5, RASSF3, 66 more genes
    nsv7063625inversion1nstd229human GRCh38 chr12: 60,220,582-64,980,713 , GRCh37.p13 chr12: 60,614,363-65,374,493 RASSF3, RPS27P24, 60 more genes
    nsv7062299inversion1nstd229human GRCh38 chr12: 62,449,536-63,818,880 , GRCh37.p13 chr12: 62,843,316-64,212,660 RXYLT1-AS1, LINC01465, 20 more genes
    nsv7062231inversion1nstd229human GRCh38 chr12: 62,212,375-66,047,637 , GRCh37.p13 chr12: 62,606,156-66,441,417 GAPDHP44, C12orf56, 73 more genes
    nsv7062117inversion1nstd229human GRCh38 chr12: 62,409,562-62,510,618 , GRCh37.p13 chr12: 62,803,342-62,904,398 MON2, USP15
    nsv7058808inversion1nstd229human GRCh38 chr12: 57,953,150-64,330,730 , GRCh37.p13 chr12: 58,346,933-64,724,510 LOC105369786, ATP23, 67 more genes
    nsv6937115copy number variation1nstd229human GRCh38 chr12: 62,490,732-62,491,084 , GRCh37.p13 chr12: 62,884,512-62,884,864 MON2
    nsv6935127copy number variation1nstd229human GRCh38 chr12: 62,421,042-62,514,497 , GRCh37.p13 chr12: 62,814,822-62,908,277 MON2
    nsv6935121copy number variation1nstd229human GRCh38 chr12: 62,305,947-62,980,827 , GRCh37.p13 chr12: 62,699,728-63,374,607 GAPDHP44, LOC105369795, 10 more genes
    nsv6934154copy number variation1nstd229human GRCh38 chr12: 62,539,485-62,540,264 , GRCh37.p13 chr12: 62,933,265-62,934,044 MON2
    nsv6929917copy number variation1nstd229human GRCh38 chr12: 62,513,694-62,514,090 , GRCh37.p13 chr12: 62,907,474-62,907,870 MON2
    nsv6927920copy number variation1nstd229human GRCh38 chr12: 62,589,043-62,592,257 , GRCh37.p13 chr12: 62,982,823-62,986,037 MON2
    nsv6923838copy number variation1nstd229human GRCh38 chr12: 62,516,532-62,521,310 , GRCh37.p13 chr12: 62,910,312-62,915,090 MON2
    nsv6923090copy number variation1nstd229human GRCh38 chr12: 62,543,790-62,543,944 , GRCh37.p13 chr12: 62,937,570-62,937,724 MON2, RNU6-399P
    nsv6921983copy number variation1nstd229human GRCh38 chr12: 62,477,305-62,670,633 , GRCh37.p13 chr12: 62,871,085-63,064,413 RNU6-399P, LINC01465, 4 more genes
    nsv6921589copy number variation1nstd229human GRCh38 chr12: 62,565,254-62,565,437 , GRCh37.p13 chr12: 62,959,034-62,959,217 MON2
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