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Items: 1 to 20 of 398

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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
    nsv7098605copy number variation1nstd102humanUncertain significance GRCh37 chrX: 15,580,028-15,864,154 , GRCh38.p12 chrX: 15,561,905-15,846,031 ACE2, CA5BP1, 8 more genes
    nsv7098592copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 14,861,689-15,870,650 , GRCh38.p12 chrX: 14,843,567-15,852,527 VEGFD, CA5BP1-CA5B, 20 more genes
    nsv7085719copy number variation1nstd229human GRCh38 chrX: 15,825,601-15,836,100 , GRCh37.p13 chrX: 15,843,724-15,854,223 AP1S2, ZRSR2
    nsv7085718copy number variation1nstd229human GRCh38 chrX: 15,789,097-15,789,587 , GRCh37.p13 chrX: 15,807,220-15,807,710 ZRSR2
    nsv7085713copy number variation1nstd229human GRCh38 chrX: 15,691,663-16,185,760 , GRCh37.p13 chrX: 15,709,786-16,203,883 INE2, CA5BP1-CA5B, 8 more genes
    nsv7085709copy number variation1nstd229human GRCh38 chrX: 15,656,438-16,128,491 , GRCh37.p13 chrX: 15,674,561-16,146,614 CA5BP1, SETP15, 8 more genes
    nsv7085708copy number variation1nstd229human GRCh38 chrX: 15,639,401-15,863,200 , GRCh37.p13 chrX: 15,657,524-15,881,323 INE2, ZRSR2, 6 more genes
    nsv7085699copy number variation1nstd229human GRCh38 chrX: 15,591,291-16,152,449 , GRCh37.p13 chrX: 15,609,414-16,170,572 CA5BP1-CA5B, ACE2-DT, 11 more genes
    nsv7085696copy number variation1nstd229human GRCh38 chrX: 15,569,980-15,802,999 , GRCh37.p13 chrX: 15,588,103-15,821,122 CLTRN, INE2, 7 more genes
    nsv7085539copy number variation1nstd229human GRCh38 chrX: 15,461,305-24,177,792 , GRCh37.p13 chrX: 15,479,428-24,195,909 LOC105373146, PIR-FIGF, 104 more genes
    nsv7085473copy number variation1nstd229human GRCh38 chrX: 15,265,887-15,855,049 , GRCh37.p13 chrX: 15,284,009-15,873,172 CLTRN, ZRSR2, 16 more genes
    nsv7085463copy number variation1nstd229human GRCh38 chrX: 15,192,575-15,841,474 , GRCh37.p13 chrX: 15,210,697-15,859,597 CA5B, AP1S2, 16 more genes
    nsv7037021inversion1nstd229human GRCh38 chrX: 14,941,162-18,599,007 , GRCh37.p13 chrX: 14,959,284-18,617,127 TXLNG, MIR4768, 54 more genes
    nsv7032726inversion1nstd229human GRCh38 chrX: 14,932,558-15,874,827 , GRCh37.p13 chrX: 14,950,680-15,892,950 INE2, HNRNPDLP5, 18 more genes
    nsv7021157inversion1nstd229human GRCh38 chrX: 14,244,684-19,508,867 , GRCh37.p13 chrX: 14,262,806-19,526,985 CA5BP1, CDKL5, 74 more genes
    nsv6636120copy number variation1nstd102humanUncertain significance GRCh37 chrX: 15,608,952-15,831,401 , GRCh38.p12 chrX: 15,590,829-15,813,278 ACE2, CA5BP1, 7 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
    nsv6634127copy number variation1nstd224human GRCh37 chrX: 15,172,189-15,867,450 , GRCh38.p12 chrX: 15,154,067-15,849,327 CLTRN, ACE2-DT, 16 more genes
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