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Items: 1 to 20 of 303

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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
    nsv7080670copy number variation1nstd229human GRCh38 chrX: 37,043,851-37,046,353 , GRCh37.p13 chrX: 37,061,924-37,064,426 , GRCh37.p13 chrX|NW_003871098.1: 859,505-862,007 FTHL18P
    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
    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
    nsv7021117inversion1nstd229human GRCh38 chrX: 37,029,574-37,567,576 , GRCh37.p13 chrX|NW_003871099.1: 1-279,382 , GRCh37.p13 chrX: 37,047,647-37,426,829 FAM47DP, FTH1P29, 6 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
    nsv6290590copy number variation1nstd102humannot provided GRCh37 chrX: 34,628,048-37,181,355 , GRCh38.p12 chrX: 34,609,931-37,322,102 CFAP47, FTH1P29, 20 more genes
    nsv6137607copy number variation1nstd213human GRCh37 chrX: 4,160,000-52,130,001 , GRCh38.p12 chrX: 4,241,959-52,386,858 NR0B1, AMELX, 630 more genes
    nsv6137606copy number variation1nstd213human GRCh37 chrX: 2,750,000-52,110,001 , GRCh38.p12 chrX: 2,831,959-52,366,858 NR0B1, AMELX, 653 more genes
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