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Items: 1 to 20 of 369

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138140copy number variation1nstd232human GRCh37.p13 chr8: 105,560,529-105,560,599 , GRCh38.p12 chr8: 104,548,301-104,548,371 LRP12
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7097886copy number variation1nstd102humanUncertain significance GRCh37 chr8: 104,412,639-106,815,766 , GRCh38.p12 chr8: 103,400,411-105,803,538 LOC105375692, LOC105375696, 28 more genes
    nsv7075711inversion1nstd229human GRCh38 chr8: 102,102,164-111,409,427 , GRCh37.p13 chr8: 103,114,392-112,421,656 LINC01181, LOC105375690, 118 more genes
    nsv7075327inversion1nstd229human GRCh38 chr8: 103,577,060-109,108,157 , GRCh37.p13 chr8: 104,589,288-110,120,386 OXR1, LOC101060000, 48 more genes
    nsv7073185inversion1nstd229human GRCh38 chr8: 104,474,583-104,489,550 , GRCh37.p13 chr8: 105,486,811-105,501,778 LRP12, MIR548A3, 1 more genes
    nsv7071528inversion1nstd229human GRCh38 chr8: 103,103,016-104,690,333 , GRCh37.p13 chr8: 104,115,244-105,702,561 LOC105375690, DCAF13, 27 more genes
    nsv7069156inversion1nstd229human GRCh38 chr8: 103,453,664-108,809,244 , GRCh37.p13 chr8: 104,465,892-109,821,473 ZFPM2-AS1, HMGB1P46, 48 more genes
    nsv6856755copy number variation1nstd229human GRCh38 chr8: 104,505,326-104,508,576 , GRCh37.p13 chr8: 105,517,554-105,520,804 LRP12
    nsv6855500copy number variation1nstd229human GRCh38 chr8: 104,190,205-104,927,632 , GRCh37.p13 chr8: 105,202,433-105,939,860 LOC105375693, LRP12, 9 more genes
    nsv6853524copy number variation1nstd229human GRCh38 chr8: 104,543,780-104,551,582 , GRCh37.p13 chr8: 105,556,008-105,563,810 LRP12
    nsv6852004copy number variation1nstd229human GRCh38 chr8: 104,567,315-104,577,397 , GRCh37.p13 chr8: 105,579,543-105,589,625 LRP12, NDUFA5P2
    nsv6851945copy number variation1nstd229human GRCh38 chr8: 104,550,105-104,553,808 , GRCh37.p13 chr8: 105,562,333-105,566,036 LRP12
    nsv6851916copy number variation1nstd229human GRCh38 chr8: 104,541,389-104,541,752 , GRCh37.p13 chr8: 105,553,617-105,553,980 LRP12
    nsv6849200copy number variation1nstd229human GRCh38 chr8: 104,540,701-104,597,800 , GRCh37.p13 chr8: 105,552,929-105,610,028 NDUFA5P2, LRP12
    nsv6847204copy number variation1nstd229human GRCh38 chr8: 104,500,001-104,505,900 , GRCh37.p13 chr8: 105,512,229-105,518,128 LRP12
    nsv6845104copy number variation1nstd229human GRCh38 chr8: 104,563,677-104,578,138 , GRCh37.p13 chr8: 105,575,905-105,590,366 NDUFA5P2, LRP12
    nsv6843161copy number variation1nstd229human GRCh38 chr8: 104,539,831-104,540,054 , GRCh37.p13 chr8: 105,552,059-105,552,282 LRP12
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
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