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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5477543copy number variation1nstd206human GRCh38 chr10: 51,699,583-51,699,665 , GRCh37.p13 chr10: 53,459,343-53,459,425 PRKG1, CSTF2T
    nsv5319080copy number variation1nstd204human GRCh37.p13 chr10: 53,189,906-54,198,554 , GRCh38.p13 chr10: 51,430,146-52,438,794 PRKG1, DKK1, 4 more genes
    nsv5318262copy number variation1nstd204human GRCh37.p13 chr10: 53,456,149-53,456,555 , GRCh38.p13 chr10: 51,696,389-51,696,795 CSTF2T, PRKG1
    nsv5254843copy number variation1nstd204human GRCh38.p13 chr10: 51,665,782-51,717,999 , GRCh37.p13 chr10: 53,425,542-53,477,759 PRKG1, CSTF2T
    nsv5251820copy number variation1nstd204human GRCh38.p13 chr10: 51,429,901-51,712,600 , GRCh37.p13 chr10: 53,189,661-53,472,360 CSTF2T, PRKG1
    nsv5246779copy number variation1nstd204human GRCh38.p13 chr10: 51,692,227-51,717,774 , GRCh37.p13 chr10: 53,451,987-53,477,534 CSTF2T, PRKG1
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4973632copy number variation1nstd200human GRCh38 chr10: 51,639,980-51,699,074 , GRCh37.p13 chr10: 53,399,740-53,458,834 PRKG1, CSTF2T
    nsv4973630copy number variation1nstd200human GRCh38 chr10: 51,537,991-52,321,754 , GRCh37.p13 chr10: 53,297,751-54,081,514 CSTF2T, PRKG1, 2 more genes
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4839412copy number variation1nstd200human GRCh37 chr10: 53,456,029-53,456,576 , GRCh38.p12 chr10: 51,696,269-51,696,816 PRKG1, CSTF2T
    nsv4832532copy number variation1nstd200human GRCh37 chr10: 53,418,193-53,544,304 , GRCh38.p12 chr10: 51,658,433-51,784,544 CSTF2T, PRKG1
    nsv4675742copy number variation1nstd102humanUncertain significance GRCh37 chr10: 53,144,955-53,811,118 , GRCh38.p12 chr10: 51,385,195-52,051,358 PRKG1, CSTF2T
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 MRLN, LOC102724778, 242 more genes
    nsv4527301copy number variation1nstd166human GRCh37.p13 chr10: 53,138,699-53,812,000 , GRCh38.p12 chr10: 51,378,939-52,052,240 CSTF2T, PRKG1
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4313384inversion1nstd166human GRCh37.p13 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , RET, 306 more genes
    nsv3972371copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 49,390,457-60,061,643 , GRCh38.p12 chr10: 45,931,517-58,301,883 CHAT, CTSLP2, 156 more genes
    nsv3964887copy number variation1nstd168human GRCh38 chr10: 51,613,152-51,738,357 , GRCh37.p13 chr10: 53,372,912-53,498,117 CSTF2T, PRKG1
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