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Items: 1 to 20 of 355

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7084483copy number variation1nstd229human GRCh38 chrX: 13,985,528-14,050,541 , GRCh37.p13 chrX: 14,003,647-14,068,660 GEMIN8
    nsv7084481copy number variation1nstd229human GRCh38 chrX: 13,979,225-14,117,676 , GRCh37.p13 chrX: 13,997,344-14,135,795 GEMIN8
    nsv7084479copy number variation1nstd229human GRCh38 chrX: 13,956,833-14,026,649 , GRCh37.p13 chrX: 13,974,952-14,044,768 GEMIN8
    nsv7084478copy number variation1nstd229human GRCh38 chrX: 13,948,326-14,074,896 , GRCh37.p13 chrX: 13,966,445-14,093,015 GEMIN8
    nsv7084469copy number variation1nstd229human GRCh38 chrX: 13,852,986-14,185,908 , GRCh37.p13 chrX: 13,871,105-14,204,030 GEMIN8, GPM6B
    nsv7079070copy number variation1nstd229human GRCh38 chrX: 13,821,418-14,306,004 , GRCh37.p13 chrX: 13,839,537-14,324,126 GPM6B, GEMIN8, 1 more genes
    nsv7079066copy number variation1nstd229human GRCh38 chrX: 13,776,500-14,422,707 , GRCh37.p13 chrX: 13,794,619-14,440,829 UBE2E4P, GPM6B, 1 more genes
    nsv7079063copy number variation1nstd229human GRCh38 chrX: 13,705,898-14,295,529 , GRCh37.p13 chrX: 13,724,017-14,313,651 OFD1, RAB9A, 4 more genes
    nsv7059136copy number variation1nstd229human GRCh38 chrX: 13,684,721-14,295,519 , GRCh37.p13 chrX: 13,702,840-14,313,641 RAB9A, TRAPPC2, 4 more genes
    nsv7023785inversion1nstd229human GRCh38 chrX: 13,472,327-15,761,537 , GRCh37.p13 chrX: 13,490,446-15,779,660 MIR6086, ACE2, 33 more genes
    nsv6636165copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,703,633-14,515,021 , GRCh38.p12 chrX: 2,785,592-14,496,899 GPX1P1, XG, 108 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634135copy number variation1nstd224human GRCh37 chrX: 2,700,157-26,836,730 , GRCh38.p12 chrX: 2,782,116-26,818,613 AMELX, ARSF, 258 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
    nsv6314786copy number variation1nstd220human GRCh37 chrX: 2,795,214-17,648,380 , GRCh38.p12 chrX: 2,877,173-17,630,260 AMELX, SHROOM2, 156 more genes
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