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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068555inversion1nstd229human GRCh38 chr8: 56,436,317-56,444,397 , GRCh37.p13 chr8: 57,348,876-57,356,956 PENK-AS1, PENK
    nsv7067508inversion1nstd229human GRCh38 chr8: 51,755,366-56,976,322 , GRCh37.p13 chr8: 52,667,926-57,888,881 CHCHD2P10, LOC105375850, 81 more genes
    nsv6855226copy number variation1nstd229human GRCh38 chr8: 56,439,003-56,439,528 , GRCh37.p13 chr8: 57,351,562-57,352,087 PENK
    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
    nsv6846005copy number variation1nstd229human GRCh38 chr8: 56,441,308-56,455,614 , GRCh37.p13 chr8: 57,353,867-57,368,173 PENK-AS1, PENK
    nsv6569954inversion1nstd223human GRCh38 chr8: 50,962,824-58,188,676 , GRCh37.p13 chr8: 51,875,384-59,101,235 LOC101929398, LOC107986888, 98 more genes
    nsv6421057copy number variation1nstd223human GRCh38 chr8: 56,423,701-56,444,400 , GRCh37.p13 chr8: 57,336,260-57,356,959 PENK, LOC105375849, 1 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
    nsv5492565copy number variation1nstd206human GRCh38 chr8: 56,442,923-56,442,999 , GRCh37.p13 chr8: 57,355,482-57,355,558 PENK
    nsv4952451copy number variation1nstd200human GRCh38 chr8: 56,443,677-56,443,839 , GRCh37.p13 chr8: 57,356,236-57,356,398 PENK, PENK-AS1
    nsv4493886mobile element insertion1nstd166human GRCh37.p13 chr8: 57,355,886-57,355,886 , GRCh38.p12 chr8: 56,443,327-56,443,327 PENK
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv3924755copy number variation1nstd102humanPathogenic NCBI36 chr8: 50,546,890-58,900,583 , GRCh37 chr8: 50,384,337-58,738,029 , GRCh38 chr8: 49,471,778-57,825,470 LOC105375849, RP1, 103 more genes
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