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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067508inversion1nstd229human GRCh38 chr8: 51,755,366-56,976,322 , GRCh37.p13 chr8: 52,667,926-57,888,881 CHCHD2P10, LOC105375850, 81 more genes
    nsv6855621copy number variation1nstd229human GRCh38 chr8: 56,499,647-56,500,861 , GRCh37.p13 chr8: 57,412,206-57,413,420 PENK-AS1, LOC101929398
    nsv6852896copy number variation1nstd229human GRCh38 chr8: 56,452,085-56,585,863 , GRCh37.p13 chr8: 57,364,644-57,498,422 LINC00968, PENK-AS1, 3 more genes
    nsv6850153copy number variation1nstd229human GRCh38 chr8: 56,342,475-56,658,333 , GRCh37.p13 chr8: 57,255,034-57,570,892 LOC105375850, SEPTIN10P1, 8 more genes
    nsv6569954inversion1nstd223human GRCh38 chr8: 50,962,824-58,188,676 , GRCh37.p13 chr8: 51,875,384-59,101,235 LOC101929398, LOC107986888, 98 more genes
    nsv6312728copy number variation1nstd102humanUncertain significance GRCh37 chr8: 56,854,419-57,906,144 , GRCh38.p12 chr8: 55,941,860-56,993,585 CERNA3, RN7SL798P, 24 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136065copy number variation1nstd213human GRCh37 chr8: 56,820,000-59,400,001 , GRCh38.p12 chr8: 55,907,441-58,487,442 LYN, MOS, 42 more genes
    nsv6136061copy number variation1nstd213human GRCh37 chr8: 54,780,000-63,060,001 , GRCh38.p12 chr8: 53,867,440-62,147,442 RAB2A, SDCBP, 117 more genes
    nsv6009173copy number variation1nstd212human GRCh38 chr8: 56,423,448-56,515,281 , GRCh37.p13 chr8: 57,336,007-57,427,840 PENK, SEPTIN10P1, 3 more genes
    nsv5724132mobile element insertion1nstd211human GRCh38 chr8: 56,494,579-56,494,579 , GRCh37.p13 chr8: 57,407,138-57,407,138 PENK-AS1, LOC101929398
    nsv5714131mobile element insertion2nstd211human GRCh38 chr8: 56,494,549-56,494,549 , GRCh37.p13 chr8: 57,407,108-57,407,108 LOC101929398, PENK-AS1
    nsv5404766mobile element insertion1nstd206human GRCh38 chr8: 56,494,549-56,494,600 , GRCh37.p13 chr8: 57,407,108-57,407,159 PENK-AS1, LOC101929398
    nsv5310116copy number variation1nstd204human GRCh37.p13 chr8: 57,405,372-57,405,492 , GRCh38.p13 chr8: 56,492,813-56,492,933 LOC101929398, PENK-AS1
    nsv5119586mobile element insertion1nstd203human GRCh38 chr8: 56,494,533-56,494,549 , GRCh37.p13 chr8: 57,407,092-57,407,108 PENK-AS1, LOC101929398
    nsv5105842mobile element insertion1nstd203human GRCh38 chr8: 56,494,538-56,494,549 , GRCh37.p13 chr8: 57,407,097-57,407,108 PENK-AS1, LOC101929398
    nsv4952455copy number variation1nstd200human GRCh38 chr8: 56,492,816-56,492,931 , GRCh37.p13 chr8: 57,405,375-57,405,490 LOC101929398, PENK-AS1
    nsv4813193copy number variation1nstd200human GRCh37 chr8: 57,405,375-57,405,490 , GRCh38.p12 chr8: 56,492,816-56,492,931 PENK-AS1, LOC101929398
    nsv4483279mobile element insertion1nstd166human GRCh37.p13 chr8: 57,411,829-57,411,829 , GRCh38.p12 chr8: 56,499,270-56,499,270 PENK-AS1, LOC101929398
    nsv4482053mobile element insertion1nstd166human GRCh37.p13 chr8: 57,407,092-57,407,092 , GRCh38.p12 chr8: 56,494,533-56,494,533 PENK-AS1, LOC101929398
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