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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094194copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 102,158,416-102,185,374 , GRCh38.p12 chr12: 101,764,638-101,791,596 GNPTAB, RNA5SP368, 2 more genes
    nsv7094118copy number variation1nstd102humanPathogenic GRCh37 chr12: 102,173,920-102,174,409 , GRCh38.p12 chr12: 101,780,142-101,780,631 RNA5SP368, GNPTAB
    nsv7094023copy number variation1nstd102humanPathogenic GRCh37 chr12: 102,157,970-102,174,409 , GRCh38.p12 chr12: 101,764,192-101,780,631 ST13P22, GNPTAB, 2 more genes
    nsv7093950copy number variation1nstd102humanPathogenic GRCh37 chr12: 102,140,932-102,224,463 , GRCh38.p12 chr12: 101,747,154-101,830,685 CHPT1, GNPTAB, 4 more genes
    nsv7093462delins1nstd102humanPathogenic GRCh38 chr12: 101,771,034-101,771,149 , GRCh37 chr12: 102,164,812-102,164,927 GNPTAB, ST13P22
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv7063562inversion1nstd229human GRCh38 chr12: 101,816,088-101,816,157 , GRCh37.p13 chr12: 102,209,866-102,209,935 GNPTAB
    nsv6937243copy number variation1nstd229human GRCh38 chr12: 101,767,778-101,962,494 , GRCh37.p13 chr12: 102,161,556-102,356,272 NENFP2, GNPTAB, 9 more genes
    nsv6936232copy number variation1nstd229human GRCh38 chr12: 101,779,692-101,780,309 , GRCh37.p13 chr12: 102,173,470-102,174,087 RNA5SP368, GNPTAB
    nsv6934655copy number variation1nstd229human GRCh38 chr12: 101,758,530-101,758,722 , GRCh37.p13 chr12: 102,152,308-102,152,500 GNPTAB
    nsv6933971copy number variation1nstd229human GRCh38 chr12: 101,806,546-101,944,077 , GRCh37.p13 chr12: 102,200,324-102,337,855 HSPE1P4, RPL9P24, 4 more genes
    nsv6933790copy number variation1nstd229human GRCh38 chr12: 101,766,713-101,770,552 , GRCh37.p13 chr12: 102,160,491-102,164,330 GNPTAB
    nsv6928446copy number variation1nstd229human GRCh38 chr12: 101,757,313-101,757,569 , GRCh37.p13 chr12: 102,151,091-102,151,347 GNPTAB
    nsv6928120copy number variation1nstd229human GRCh38 chr12: 101,779,786-101,995,724 , GRCh37.p13 chr12: 102,173,564-102,389,502 RNU6-172P, DRAM1, 8 more genes
    nsv6926679copy number variation1nstd229human GRCh38 chr12: 101,785,450-101,956,134 , GRCh37.p13 chr12: 102,179,228-102,349,912 RNU6-1183P, LOC107984548, 6 more genes
    nsv6923201copy number variation1nstd229human GRCh38 chr12: 101,772,946-101,773,075 , GRCh37.p13 chr12: 102,166,724-102,166,853 ST13P22, GNPTAB
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6919187copy number variation1nstd229human GRCh38 chr12: 101,763,806-101,763,976 , GRCh37.p13 chr12: 102,157,584-102,157,754 RNU6-101P, GNPTAB
    nsv6918584copy number variation1nstd229human GRCh38 chr12: 101,747,852-101,747,913 , GRCh37.p13 chr12: 102,141,630-102,141,691 GNPTAB, CHPT1
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