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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099190copy number variation1nstd231human GRCh38.p12 chr1: 28,757,517-29,693,149 , GRCh37 chr1: 29,084,029-30,165,996 EPB41, OPRD1, 9 more genes
    nsv7057641inversion1nstd229human GRCh38 chr1: 28,777,628-30,518,986 , GRCh37.p13 chr1: 29,104,140-30,991,833 LOC105378618, LINC01648, 11 more genes
    nsv7051655inversion1nstd229human GRCh38 chr1: 29,022,571-29,214,533 , GRCh37.p13 chr1: 29,349,083-29,541,045 EPB41, MECR, 2 more genes
    nsv7045885inversion1nstd229human GRCh38 chr1: 29,025,951-29,214,353 , GRCh37.p13 chr1: 29,352,463-29,540,865 TMEM200B, EPB41, 2 more genes
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv6648556copy number variation1nstd229human GRCh38 chr1: 29,223,823-29,224,266 , GRCh37.p13 chr1: 29,550,335-29,550,778 MECR
    nsv6648555copy number variation1nstd229human GRCh38 chr1: 29,220,059-29,225,796 , GRCh37.p13 chr1: 29,546,571-29,552,308 MECR
    nsv6648553copy number variation1nstd229human GRCh38 chr1: 29,180,901-29,330,500 , GRCh37.p13 chr1: 29,507,413-29,657,012 LINC01756, MECR, 2 more genes
    nsv6648410copy number variation1nstd229human GRCh38 chr1: 29,218,667-29,223,380 , GRCh37.p13 chr1: 29,545,179-29,549,892 MECR
    nsv6648409copy number variation1nstd229human GRCh38 chr1: 29,184,234-29,203,213 , GRCh37.p13 chr1: 29,510,746-29,529,725 MECR
    nsv6648357copy number variation1nstd229human GRCh38 chr1: 29,224,725-29,226,719 , GRCh37.p13 chr1: 29,551,237-29,553,231 MECR
    nsv6648356copy number variation1nstd229human GRCh38 chr1: 29,199,551-29,203,873 , GRCh37.p13 chr1: 29,526,063-29,530,385 MECR
    nsv6547430inversion1nstd223human GRCh38 chr1: 29,022,567-29,214,536 , GRCh37.p13 chr1: 29,349,079-29,541,048 EPB41, SRSF4, 2 more genes
    nsv6546491inversion1nstd223human GRCh38 chr1: 29,225,999-29,227,029 , GRCh37.p13 chr1: 29,552,511-29,553,541 MECR
    nsv6333404copy number variation1nstd223human GRCh38 chr1: 29,224,725-29,226,719 , GRCh37.p13 chr1: 29,551,237-29,553,231 MECR
    nsv6327646copy number variation1nstd223human GRCh38 chr1: 29,218,667-29,223,375 , GRCh37.p13 chr1: 29,545,179-29,549,887 MECR
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv5983902copy number variation1nstd212human GRCh38 chr1: 29,214,109-29,214,408 , GRCh37.p13 chr1: 29,540,621-29,540,920 MECR
    nsv5976208inversion1nstd209human GRCh38 chr1: 29,022,566-29,214,534 , GRCh37.p13 chr1: 29,349,078-29,541,046 EPB41, SRSF4, 2 more genes
    nsv5562353sequence alteration1nstd206human GRCh38 chr1: 29,022,565-29,214,535 , GRCh37.p13 chr1: 29,349,077-29,541,047 EPB41, SRSF4, 2 more genes
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