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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907408copy number variation1nstd209human GRCh38 chr6: 34,764,357-34,764,543 , GRCh37.p13 chr6: 34,732,134-34,732,320 SNRPC
    nsv5463167copy number variation1nstd206human GRCh38 chr6: 34,754,560-34,756,268 , GRCh37.p13 chr6: 34,722,337-34,724,045 SNRPC
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv4940837copy number variation1nstd200human GRCh38 chr6: 34,754,725-34,756,219 , GRCh37.p13 chr6: 34,722,502-34,723,996 SNRPC
    nsv4940836copy number variation1nstd200human GRCh38 chr6: 34,749,053-34,755,166 , GRCh37.p13 chr6: 34,716,830-34,722,943 SNRPC
    nsv4934609copy number variation1nstd200human GRCh38 chr6: 34,754,733-34,919,575 , GRCh37.p13 chr6: 34,722,510-34,887,352 RNY3P15, SNRPC, 3 more genes
    nsv4815975copy number variation1nstd200human GRCh37 chr6: 34,728,981-34,729,381 , GRCh38.p12 chr6: 34,761,204-34,761,604 SNRPC
    nsv4815974copy number variation1nstd200human GRCh37 chr6: 34,722,484-34,724,021 , GRCh38.p12 chr6: 34,754,707-34,756,244 SNRPC
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4715008translocation1nstd195human GRCh37 chr5: 75,673,318-75,673,318 , GRCh37 chr6: 34,741,700-34,741,700 , GRCh38.p12 chr5: 76,377,493-76,377,493 , GRCh38.p12 chr6: 34,773,923-34,773,923 SNRPC, SNRPCP2
    nsv4707502translocation1nstd195human GRCh37 chr5: 75,673,318-75,673,318 , GRCh37 chr6: 34,741,701-34,741,701 , GRCh38.p12 chr5: 76,377,493-76,377,493 , GRCh38.p12 chr6: 34,773,924-34,773,924 SNRPC, SNRPCP2
    nsv4679436copy number variation1nstd189human GRCh37.p13 chr6: 34,340,307-35,087,160 , GRCh38.p12 chr6: 34,372,530-35,119,383 RPS10, SNRPC, 18 more genes
    nsv4592495copy number variation1nstd183human GRCh37 chr6: 34,723,735-34,887,316 , GRCh38.p12 chr6: 34,755,958-34,919,539 ANKS1A, BLTP3A, 3 more genes
    nsv4488459mobile element insertion1nstd166human GRCh37.p13 chr6: 34,741,128-34,741,128 , GRCh38.p12 chr6: 34,773,351-34,773,351 SNRPC
    nsv4455893copy number variation1nstd102humanUncertain significance GRCh37 chr6: 34,630,244-35,087,148 , GRCh38.p12 chr6: 34,662,467-35,119,371 HSPE1P11, RPS10P13, 11 more genes
    nsv4394547copy number variation1nstd174human GRCh37 chr6: 34,723,723-34,961,360 , GRCh38.p12 chr6: 34,755,946-34,993,583 BLTP3A, RNY3P15, 3 more genes
    nsv4388514copy number variation1nstd173human GRCh37 chr6: 34,717,275-34,887,258 , GRCh38.p12 chr6: 34,749,498-34,919,481 SNRPC, ANKS1A, 3 more genes
    nsv4382344copy number variation2nstd173human GRCh37 chr6: 34,741,917-34,887,258 , GRCh38.p12 chr6: 34,774,140-34,919,481 BLTP3A, TAF11, 3 more genes
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