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Items: 1 to 20 of 321

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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
    nsv7091701copy number variation1nstd229human GRCh38 chrX: 36,923,645-37,039,479 , GRCh37.p13 chrX|NW_003871098.1: 739,299-855,133 , GRCh37.p13 chrX: 36,941,718-37,057,552 FAM47C, TFDP1P2, 1 more genes
    nsv7080662copy number variation1nstd229human GRCh38 chrX: 36,986,461-36,986,488 , GRCh37.p13 chrX: 37,004,534-37,004,561 , GRCh37.p13 chrX|NW_003871098.1: 802,115-802,142 LOC100422408
    nsv7080661copy number variation1nstd229human GRCh38 chrX: 36,984,750-36,984,961 , GRCh37.p13 chrX|NW_003871098.1: 800,404-800,615 , GRCh37.p13 chrX: 37,002,823-37,003,034 LOC100422408
    nsv7080660copy number variation1nstd229human GRCh38 chrX: 36,976,730-37,003,624 , GRCh37.p13 chrX: 36,994,803-37,021,697 , GRCh37.p13 chrX|NW_003871098.1: 792,384-819,278 LOC100422408
    nsv7080652copy number variation1nstd229human GRCh38 chrX: 36,821,742-37,799,642 , GRCh37.p13 chrX|NW_003871099.1: 1-511,448 , GRCh37.p13 chrX: 36,839,815-37,658,895 FTHL18P, FAM47DP, 12 more genes
    nsv7080651copy number variation1nstd229human GRCh38 chrX: 36,820,026-37,001,646 , GRCh37.p13 chrX: 36,838,099-37,019,719 , GRCh37.p13 chrX|NW_003871098.1: 635,680-817,300 TFDP1P2, LOC100422408
    nsv7037966inversion1nstd229human GRCh38 chrX: 36,986,100-37,575,172 , GRCh37.p13 chrX: 37,004,173-37,434,425 FTH1P19, FAM47C, 9 more genes
    nsv7032924inversion1nstd229human GRCh38 chrX: 34,355,734-41,258,887 , GRCh37.p13 chrX: 34,373,851-41,118,140 IMPDH1P2, RPL32P36, 81 more genes
    nsv7024010inversion1nstd229human GRCh38 chrX: 36,983,779-37,673,667 , GRCh37.p13 chrX|NW_003871099.1: 1-385,473 , GRCh37.p13 chrX: 37,001,852-37,532,920 FTH1P28, FTH1P29, 9 more genes
    nsv7019905inversion1nstd229human GRCh38 chrX: 36,588,447-37,065,470 , GRCh37.p13 chrX|NW_003871098.1: 404,101-881,124 , GRCh37.p13 chrX: 36,606,521-37,083,543 FAM47C, FTHL18P, 4 more genes
    nsv6636670copy number variation1nstd102humanPathogenic GRCh37 chrX: 32,419,533-37,487,291 , GRCh38.p12 chrX: 32,401,416-37,628,038 FAM47B, FAM47A, 36 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6633814copy number variation1nstd224human GRCh37 chrX: 36,885,729-37,267,016 , GRCh38.p12 chrX: 36,867,656-37,407,763 PRRG1, TFDP1P2, 5 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 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
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6315330copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-57,841,304 , GRCh38.p12 chrX: 251,879-57,814,871 NPM1P9, UBE2E4P, 799 more genes
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