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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144021insertion1nstd232human GRCh37.p13 chr1: 109,495,134-109,495,134 , GRCh38.p12 chr1: 108,952,512-108,952,512 CLCC1
    nsv7099223copy number variation1nstd231human GRCh38.p12 chr1: 108,551,579-110,710,631 , GRCh37 chr1: 109,094,201-111,253,253 ALX3, AMPD2, 74 more genes
    nsv7095739copy number variation1nstd102humanPathogenic GRCh37 chr1: 108,679,275-111,674,176 , GRCh38.p12 chr1: 108,136,653-111,131,554 RPL7L1P21, GSTM4, 90 more genes
    nsv7095693copy number variation1nstd102humanUncertain significance GRCh37 chr1: 108,679,275-109,493,059 , GRCh38.p12 chr1: 108,136,653-108,950,437 AKNAD1, LOC105378890, 18 more genes
    nsv7095314copy number variation1nstd102humanUncertain significance GRCh37 chr1: 109,428,145-109,817,590 , GRCh38.p12 chr1: 108,885,523-109,274,968 SARS1, LOC107985160, 15 more genes
    nsv7054448inversion1nstd229human GRCh38 chr1: 108,867,945-109,235,536 , GRCh37.p13 chr1: 109,410,567-109,778,158 SARS1, GPSM2, 14 more genes
    nsv7048509inversion1nstd229human GRCh38 chr1: 108,319,829-109,244,823 , GRCh37.p13 chr1: 108,862,451-109,787,445 RPS27P6, ST13P21, 30 more genes
    nsv7044488inversion1nstd229human GRCh38 chr1: 100,052,919-109,025,639 , GRCh37.p13 chr1: 100,518,475-109,568,261 LOC102723784, DNAJA1P5, 109 more genes
    nsv6639735copy number variation1nstd229human GRCh38 chr1: 108,930,496-108,930,627 , GRCh37.p13 chr1: 109,473,118-109,473,249 GPSM2, CLCC1
    nsv6639733copy number variation1nstd229human GRCh38 chr1: 108,886,561-109,266,572 , GRCh37.p13 chr1: 109,429,183-109,809,194 TMEM167B-DT, CFAP276, 15 more genes
    nsv6639721copy number variation1nstd229human GRCh38 chr1: 108,756,469-109,410,478 , GRCh37.p13 chr1: 109,299,091-109,953,100 PSMA5, STXBP3, 24 more genes
    nsv6639647copy number variation1nstd229human GRCh38 chr1: 108,952,201-108,957,200 , GRCh37.p13 chr1: 109,494,823-109,499,822 CLCC1
    nsv6639646copy number variation1nstd229human GRCh38 chr1: 108,945,537-108,945,698 , GRCh37.p13 chr1: 109,488,159-109,488,320 CLCC1
    nsv6639559copy number variation1nstd229human GRCh38 chr1: 108,953,801-108,960,000 , GRCh37.p13 chr1: 109,496,423-109,502,622 CLCC1
    nsv6639543copy number variation1nstd229human GRCh38 chr1: 108,780,593-109,355,741 , GRCh37.p13 chr1: 109,323,215-109,898,363 STXBP3, TMEM167B-DT, 22 more genes
    nsv6639542copy number variation1nstd229human GRCh38 chr1: 108,770,665-108,967,507 , GRCh37.p13 chr1: 109,313,287-109,510,129 SPATA42, LOC105378891, 4 more genes
    nsv6639419copy number variation1nstd229human GRCh38 chr1: 108,866,262-109,183,745 , GRCh37.p13 chr1: 109,408,884-109,726,367 CLCC1, GPSM2, 13 more genes
    nsv6639418copy number variation1nstd229human GRCh38 chr1: 108,842,021-109,295,218 , GRCh37.p13 chr1: 109,384,643-109,837,840 PSRC1, AKNAD1, 19 more genes
    nsv6639410copy number variation1nstd229human GRCh38 chr1: 108,787,709-108,950,012 , GRCh37.p13 chr1: 109,330,331-109,492,634 STXBP3, AKNAD1, 4 more genes
    nsv6636931copy number variation1nstd102humanUncertain significance GRCh37 chr1: 109,371,874-109,906,234 , GRCh38.p12 chr1: 108,829,252-109,363,612 CELSR2, TAF13, 21 more genes
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