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Items: 1 to 20 of 277

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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
    nsv7081112copy number variation1nstd229human GRCh38 chrX: 55,936,077-55,979,912 , GRCh37.p13 chrX: 55,962,510-56,006,345 GOT2P6, KLF8
    nsv7081092copy number variation1nstd229human GRCh38 chrX: 55,783,192-56,282,759 , GRCh37.p13 chrX: 55,809,625-56,309,192 KLF8, GOT2P6, 1 more genes
    nsv7025237inversion1nstd229human GRCh38 chrX: 50,557,525-57,228,328 , GRCh37.p13 chrX|NW_004070877.1: 270,640-4,110,759 , GRCh37.p13 chrX: 50,300,525-54,424,077 UBQLN2, IPO7P1, 141 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
    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
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 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
    nsv6138507copy number variation1nstd206human GRCh38 chrX: 55,728,000-56,175,100 , GRCh37.p13 chrX: 55,754,433-56,201,533 RRAGB, KLF8, 1 more genes
    nsv6137620copy number variation1nstd213human GRCh37 chrX: 55,770,000-56,380,001 , GRCh38.p12 chrX: 55,743,567-56,353,568 RRAGB, KLF8, 2 more genes
    nsv6137619copy number variation1nstd213human GRCh37 chrX: 52,520,000-58,560,001 , GRCh38.p12 chrX: 52,523,686-58,533,568 ACTG1P10, ALAS2, 106 more genes
    nsv6137618copy number variation1nstd213human GRCh37 chrX: 52,510,000-58,560,001 , GRCh38.p12 chrX: 52,523,686-58,533,568 ACTG1P10, ALAS2, 106 more genes
    nsv6137617copy number variation1nstd213human GRCh37 chrX: 52,480,000-58,240,001 , GRCh38.p12 chrX: 52,523,686-58,213,567 ACTG1P10, ALAS2, 106 more genes
    nsv6137402copy number variation1nstd213human GRCh37 chrX: 55,560,000-58,140,001 , GRCh38.p12 chrX: 55,533,567-58,113,567 MTHFD1P1, ZXDA, 22 more genes
    nsv6137401copy number variation1nstd213human GRCh37 chrX: 55,480,000-58,560,001 , GRCh38.p12 chrX: 55,453,567-58,533,568 MTHFD1P1, ZXDA, 26 more genes
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