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Items: 1 to 20 of 298

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7092074copy number variation1nstd229human GRCh38 chrX: 57,679,801-57,691,900 , GRCh37.p13 chrX: 57,706,234-57,718,333 NLRP2B
    nsv7092073copy number variation1nstd229human GRCh38 chrX: 57,676,197-57,994,729 , GRCh37.p13 chrX: 57,702,630-58,021,163 MYCLP2, KRT8P17, 3 more genes
    nsv7092072copy number variation1nstd229human GRCh38 chrX: 57,668,350-57,804,768 , GRCh37.p13 chrX: 57,694,783-57,831,201 NLRP2B, LOC107985708, 1 more genes
    nsv7088288copy number variation1nstd229human GRCh38 chrX: 57,662,801-57,804,800 , GRCh37.p13 chrX: 57,689,234-57,831,233 MDH1P1, NLRP2B, 1 more genes
    nsv7088231copy number variation1nstd229human GRCh38 chrX: 57,216,637-57,999,292 , GRCh37.p13 chrX: 57,243,070-58,025,726 KRT8P17, ZXDA, 8 more genes
    nsv7088230copy number variation1nstd229human GRCh38 chrX: 57,216,078-57,698,668 , GRCh37.p13 chrX: 57,242,511-57,725,101 FAAH2, MTHFD1P1, 4 more genes
    nsv7081251copy number variation1nstd229human GRCh38 chrX: 56,856,775-57,906,091 , GRCh37.p13 chrX: 56,883,208-57,932,525 MDH1P1, ZXDA, 10 more genes
    nsv7024436inversion1nstd229human GRCh38 chrX: 57,096,986-57,848,955 , GRCh37.p13 chrX: 57,123,419-57,875,388 PPP1R11P2, ZXDB, 7 more genes
    nsv7024182inversion1nstd229human GRCh38 chrX: 55,283,275-57,909,590 , GRCh37.p13 chrX: 55,309,708-57,936,024 UBQLN2, USP51, 27 more genes
    nsv7020530inversion1nstd229human GRCh38 chrX: 56,736,354-57,752,027 , GRCh37.p13 chrX: 56,762,787-57,778,460 UQCRBP1, LOC107985708, 10 more genes
    nsv7019262inversion1nstd229human GRCh38 chrX: 57,080,814-57,780,738 , GRCh37.p13 chrX: 57,107,247-57,807,171 NLRP2B, MTHFD1P1, 7 more genes
    nsv6636248copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 53,731,940-63,932,866 , GRCh38.p12 chrX: 53,704,997-64,712,986 ALAS2, FGD1, 89 more genes
    nsv6636004copy number variation1nstd102humanPathogenic GRCh38 chrX: 57,537,466-65,512,709 , GRCh37.p13 chrX: 57,563,899-64,732,589 ZC4H2, ZC3H12B, 43 more genes
    nsv6634261copy number variation1nstd224human GRCh37 chrX: 56,889,389-58,389,872 , GRCh38.p12 chrX: 56,862,956-58,363,439 SPIN3, NLRP2B, 12 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634158copy number variation1nstd224human GRCh37 chrX: 57,628,448-58,403,144 , GRCh38.p12 chrX: 57,602,015-58,376,711 ZXDA, NLRP2B, 4 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
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