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Items: 1 to 20 of 14582

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123072copy number variation1nstd186human GRCh37 chr8: 8,679,911-8,680,203 , GRCh38.p12 chr8|NW_018654717.1: 4,529,303-4,529,595 , GRCh38.p12 chr8: 8,822,401-8,822,693 MFHAS1
    nsv6117154mobile element insertion1nstd186human GRCh37 chr8: 11,225,300-11,225,300 , GRCh38.p12 chr8: 11,367,791-11,367,791 , GRCh38.p12 chr8|NW_018654717.1: 1,979,060-1,979,060 FAM167A-AS1, TDH
    nsv6114883mobile element insertion1nstd186human GRCh37 chr8: 10,132,604-10,132,655 , GRCh38.p12 chr8: 10,275,094-10,275,145 , GRCh38.p12 chr8|NW_018654717.1: 3,071,916-3,071,967 MSRA
    nsv6113897mobile element insertion1nstd186human GRCh37 chr8: 9,807,901-9,807,952 , GRCh38.p12 chr8: 9,950,391-9,950,442 , GRCh38.p12 chr8|NW_018654717.1: 3,397,953-3,398,003 0
    nsv6112660copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 11,403,560-11,853,760 , GRCh38.p12 chr8: 11,546,051-11,996,251 , GRCh38.p12 chr8|NW_018654717.1: 1,351,766-1,802,047 BLK, CTSB, 19 more genes
    nsv5388452copy number variation1nstd186human GRCh37 chr8: 9,497,901-9,500,952 , GRCh38.p12 chr8|NW_018654717.1: 3,708,058-3,711,109 , GRCh38.p12 chr8: 9,640,391-9,643,442 TNKS
    nsv5388413copy number variation1nstd186human GRCh37 chr8: 9,497,901-9,500,950 , GRCh38.p12 chr8|NW_018654717.1: 3,708,060-3,711,109 , GRCh38.p12 chr8: 9,640,391-9,643,440 TNKS
    nsv5388248copy number variation1nstd186human GRCh37 chr8: 11,494,927-11,495,286 , GRCh38.p12 chr8: 11,637,418-11,637,777 , GRCh38.p12 chr8|NW_018654717.1: 1,710,270-1,710,616 LOC105379242
    nsv5388195copy number variation1nstd186human GRCh37 chr8: 12,233,487-12,236,117 , GRCh38.p12 chr8: 12,375,978-12,378,608 , GRCh38.p12 chr8|NW_018654717.1: 1,209,868-1,212,494 LOC649352, FAM66A, 1 more genes
    nsv5387954copy number variation3nstd186human GRCh37 chr8: 11,596,931-11,597,266 , GRCh38.p12 chr8: 11,739,422-11,739,757 , GRCh38.p12 chr8|NW_018654717.1: 1,608,322-1,608,657 GATA4
    nsv5387842copy number variation2nstd186human GRCh37 chr8: 6,648,218-6,648,320 , GRCh38.p12 chr8|NW_018654717.1: 185,966-186,068 , GRCh38.p12 chr8: 6,790,697-6,790,799 0
    nsv5387750copy number variation3nstd186human GRCh37 chr8: 9,054,978-9,062,720 , GRCh38.p12 chr8: 9,197,468-9,205,210 , GRCh38.p12 chr8|NW_018654717.1: 4,146,362-4,154,103 LOC101929128
    nsv5387433copy number variation1nstd186human GRCh37 chr8: 10,883,662-10,884,322 , GRCh38.p12 chr8: 11,026,152-11,026,812 , GRCh38.p12 chr8|NW_018654717.1: 2,320,190-2,321,073 XKR6, LOC112268405
    nsv5387358copy number variation2nstd186human GRCh37 chr8: 8,385,907-8,386,944 , GRCh38.p12 chr8|NW_018654717.1: 4,822,647-4,823,684 , GRCh38.p12 chr8: 8,528,397-8,529,434 0
    nsv5387332copy number variation1nstd186human GRCh37 chr8: 8,997,885-8,998,112 , GRCh38.p12 chr8|NW_018654717.1: 4,211,028-4,211,255 , GRCh38.p12 chr8: 9,140,375-9,140,602 PPP1R3B
    nsv5386684copy number variation1nstd186human GRCh37 chr8: 11,492,308-11,495,244 , GRCh38.p12 chr8: 11,634,799-11,637,735 , GRCh38.p12 chr8|NW_018654717.1: 1,710,312-1,713,235 LOC105379242
    nsv5386520copy number variation1nstd186human GRCh37 chr8: 11,494,993-11,495,211 , GRCh38.p12 chr8: 11,637,484-11,637,702 , GRCh38.p12 chr8|NW_018654717.1: 1,710,345-1,710,550 LOC105379242
    nsv5385622copy number variation1nstd186human GRCh37 chr8: 10,883,662-10,884,306 , GRCh38.p12 chr8: 11,026,152-11,026,796 , GRCh38.p12 chr8|NW_018654717.1: 2,320,206-2,321,073 XKR6, LOC112268405
    nsv5385569copy number variation2nstd186human GRCh37 chr8: 11,036,108-11,036,222 , GRCh38.p12 chr8|NW_018654717.1: 2,168,188-2,168,302 , GRCh38.p12 chr8: 11,178,599-11,178,713 XKR6
    nsv5383536mobile element deletion2nstd186human GRCh37 chr8: 10,216,077-10,216,390 , GRCh38.p12 chr8|NW_018654717.1: 2,988,204-2,988,491 , GRCh38.p12 chr8: 10,358,567-10,358,880 MSRA
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