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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv6639741copy number variation1nstd229human GRCh38 chr1: 109,097,401-109,356,500 , GRCh37.p13 chr1: 109,640,023-109,899,122 ELAPOR1, CELSR2, 8 more genes
    nsv6639737copy number variation1nstd229human GRCh38 chr1: 108,995,726-109,154,741 , GRCh37.p13 chr1: 109,538,348-109,697,363 TMEM167B, SCARNA2, 9 more genes
    nsv6639736copy number variation1nstd229human GRCh38 chr1: 108,994,101-109,359,800 , GRCh37.p13 chr1: 109,536,723-109,902,422 LOC100420092, PSRC1, 14 more genes
    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
    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
    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
    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
    nsv6636625copy number variation1nstd102humanUncertain significance GRCh37 chr1: 109,350,810-109,838,970 , GRCh38.p12 chr1: 108,808,188-109,296,348 CELSR2, RANP5, 21 more genes
    nsv6636374copy number variation1nstd102humanUncertain significance GRCh37 chr1: 109,396,971-109,807,574 , GRCh38.p12 chr1: 108,854,349-109,264,952 GPSM2, LOC107985160, 17 more genes
    nsv6544588inversion1nstd223human GRCh38 chr1: 108,867,933-109,235,536 , GRCh37.p13 chr1: 109,410,555-109,778,158 TMEM167B-DT, CFAP276, 14 more genes
    nsv6330458copy number variation1nstd223human GRCh38 chr1: 108,984,462-109,187,303 , GRCh37.p13 chr1: 109,527,084-109,729,925 ELAPOR1, RPL17P7, 11 more genes
    nsv6325446copy number variation1nstd223human GRCh38 chr1: 109,088,622-109,089,982 , GRCh37.p13 chr1: 109,631,244-109,632,604 TMEM167B, TMEM167B-DT
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
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