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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7047929inversion1nstd229human GRCh38 chr6: 2,249,577-5,332,355 , GRCh37.p13 chr6: 2,249,811-5,332,588 LOC107986561, NQO2-AS1, 67 more genes
    nsv7044205inversion1nstd229human GRCh38 chr6: 2,472,898-4,774,625 , GRCh37.p13 chr6: 2,473,132-4,774,859 TOMM5P1, PXDC1, 56 more genes
    nsv6792056copy number variation1nstd229human GRCh38 chr6: 3,608,201-3,857,700 , GRCh37.p13 chr6: 3,608,435-3,857,934 LOC100507336, TOMM5P1, 3 more genes
    nsv6791971copy number variation1nstd229human GRCh38 chr6: 3,403,601-4,596,900 , GRCh37.p13 chr6: 3,403,835-4,597,134 ECI2-DT, PRPF4B, 24 more genes
    nsv6785298copy number variation1nstd229human GRCh38 chr6: 2,759,301-4,105,800 , GRCh37.p13 chr6: 2,759,535-4,106,034 LOC107986557, SERPINB9-AS1, 39 more genes
    nsv6783631copy number variation1nstd229human GRCh38 chr6: 3,836,457-3,841,430 , GRCh37.p13 chr6: 3,836,691-3,841,664 FAM50B
    nsv6780010copy number variation1nstd229human GRCh38 chr6: 3,816,935-3,883,996 , GRCh37.p13 chr6: 3,817,169-3,884,230 FAM50B, LOC107986557
    nsv6779843copy number variation1nstd229human GRCh38 chr6: 3,839,358-3,845,840 , GRCh37.p13 chr6: 3,839,592-3,846,074 FAM50B, LOC107986557
    nsv6631058copy number variation1nstd224human GRCh37 chr6: 3,779,243-4,031,998 , GRCh38.p12 chr6: 3,779,009-4,031,764 PRPF4B, CRIPTOP4, 5 more genes
    nsv6404987copy number variation1nstd223human GRCh38 chr6: 3,836,457-3,841,426 , GRCh37.p13 chr6: 3,836,691-3,841,660 FAM50B
    nsv6313679copy number variation1nstd102humanPathogenic GRCh37 chr6: 383,951-3,898,619 , GRCh38.p12 chr6: 383,951-3,898,385 SERPINB9P1, LOC101927691, 59 more genes
    nsv6136505copy number variation1nstd213human GRCh37 chr6: 380,000-11,010,001 , GRCh38.p12 chr6: 380,000-11,009,768 BMP6, BPHL, 178 more genes
    nsv6135513copy number variation1nstd213human GRCh37 chr6: 380,000-10,980,001 , GRCh38.p12 chr6: 380,000-10,979,768 BMP6, BPHL, 178 more genes
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv4949375copy number variation1nstd200human GRCh38 chr6: 3,816,935-3,883,996 , GRCh37.p13 chr6: 3,817,169-3,884,230 FAM50B, LOC107986557
    nsv4675745copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,770,033-3,987,451 , GRCh38.p12 chr6: 3,769,799-3,987,217 LOC107986558, GLRX3P2, 4 more genes
    nsv4570351sequence alteration1nstd166human GRCh37.p13 chr6: 3,851,820-3,853,212 , GRCh38.p12 chr6: 3,851,586-3,852,978 FAM50B
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv3972110copy number variation1nstd102humanLikely benign GRCh37 chr6: 3,768,839-3,972,010 , GRCh38.p12 chr6: 3,768,605-3,971,776 CRIPTOP4, LOC107986558, 3 more genes
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