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Items: 1 to 20 of 315

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145807insertion1nstd232human GRCh37.p13 chrX: 73,049,068-73,049,068 , GRCh38.p12 chrX: 73,829,233-73,829,233 XIST, TSIX
    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
    nsv7092445copy number variation1nstd229human GRCh38 chrX: 73,850,701-73,967,000 , GRCh37.p13 chrX: 73,070,536-73,186,835 FXYD6P3, XIST, 1 more genes
    nsv7092444copy number variation1nstd229human GRCh38 chrX: 73,842,799-73,842,914 , GRCh37.p13 chrX: 73,062,634-73,062,749 XIST
    nsv7092443copy number variation1nstd229human GRCh38 chrX: 73,840,900-74,086,451 , GRCh37.p13 chrX: 73,060,735-73,306,286 RPSAP14, FTX, 4 more genes
    nsv7092442copy number variation1nstd229human GRCh38 chrX: 73,836,533-73,836,593 , GRCh37.p13 chrX: 73,056,368-73,056,428 XIST
    nsv7092441copy number variation1nstd229human GRCh38 chrX: 73,836,530-73,895,436 , GRCh37.p13 chrX: 73,056,365-73,115,271 FXYD6P3, XIST
    nsv7092440copy number variation1nstd229human GRCh38 chrX: 73,827,257-73,827,378 , GRCh37.p13 chrX: 73,047,092-73,047,213 TSIX, XIST
    nsv7092439copy number variation1nstd229human GRCh38 chrX: 73,822,748-73,823,110 , GRCh37.p13 chrX: 73,042,583-73,042,945 TSIX, XIST
    nsv7092438copy number variation1nstd229human GRCh38 chrX: 73,822,075-73,822,561 , GRCh37.p13 chrX: 73,041,910-73,042,396 TSIX, XIST
    nsv7092437copy number variation1nstd229human GRCh38 chrX: 73,818,347-73,821,574 , GRCh37.p13 chrX: 73,038,182-73,041,409 XIST, TSIX
    nsv7092423copy number variation1nstd229human GRCh38 chrX: 73,669,580-73,905,018 , GRCh37.p13 chrX: 72,889,415-73,124,853 XIST, FXYD6P3, 3 more genes
    nsv7092385copy number variation1nstd229human GRCh38 chrX: 73,568,179-73,917,249 , GRCh37.p13 chrX: 72,788,015-73,137,084 XIST, FXYD6P3, 3 more genes
    nsv7018592inversion1nstd229human GRCh38 chrX: 71,642,458-75,115,067 , GRCh37.p13 chrX: 70,862,308-74,334,902 RN7SL648P, LOC101059915, 83 more genes
    nsv6636591copy number variation1nstd102humanUncertain significance GRCh37 chrX: 72,024,935-73,087,982 , GRCh38.p12 chrX: 72,805,101-73,868,147 FAM236A, CHIC1, 22 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 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
    nsv6315332copy number variation1nstd102humanPathogenic GRCh37 chrX: 62,685,885-155,233,731 , GRCh38.p12 chrX: 63,466,005-156,004,066 MAGT1, TAFAZZIN, 1337 more genes
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