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Items: 1 to 20 of 299

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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
    nsv7083657copy number variation1nstd229human GRCh38 chrX: 124,169,201-124,213,200 , GRCh37.p13 chrX: 123,303,051-123,347,050 ZIK1P1, HSPA8P20
    nsv7083650copy number variation1nstd229human GRCh38 chrX: 124,119,401-124,173,100 , GRCh37.p13 chrX: 123,253,251-123,306,950 ZIK1P1
    nsv7083638copy number variation1nstd229human GRCh38 chrX: 123,995,175-124,183,553 , GRCh37.p13 chrX: 123,129,025-123,317,403 ZIK1P1, STAG2
    nsv7083371copy number variation1nstd229human GRCh38 chrX: 121,591,286-126,454,661 , GRCh37.p13 chrX: 120,725,140-125,588,644 RNU7-69P, SH2D1A, 31 more genes
    nsv7055412inversion1nstd229human GRCh38 chrX: 124,173,096-124,317,582 , GRCh37.p13 chrX: 123,306,946-123,451,432 NPM1P34, HSPA8P20, 1 more genes
    nsv7043222inversion1nstd229human GRCh38 chrX: 124,169,171-124,200,915 , GRCh37.p13 chrX: 123,303,021-123,334,765 ZIK1P1
    nsv7041243inversion1nstd229human GRCh38 chrX: 124,055,047-124,220,432 , GRCh37.p13 chrX: 123,188,897-123,354,282 HSPA8P20, ZIK1P1, 1 more genes
    nsv6637110copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,773,699-123,323,939 , GRCh38.p12 chrX: 123,639,848-124,190,089 XIAP, STAG2, 9 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315429copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,670,699-155,233,731 , GRCh38.p12 chrX: 78,415,202-156,004,066 H2AB1, GPR174, 1081 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
    nsv6315380copy number variation1nstd102humanPathogenic GRCh37 chrX: 122,855,926-123,438,005 , GRCh38.p12 chrX: 123,722,076-124,304,155 PARD6BP1, STAG2-AS1, 11 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
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6315159copy number variation1nstd102humanPathogenic GRCh38 chrX: 123,221,813-124,917,630 , GRCh37.p13 chrX: 122,355,664-124,051,479 STAG2-AS1, FERP1, 21 more genes
    nsv6313138copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 122,318,388-123,505,241 , GRCh38.p12 chrX: 123,184,536-124,371,391 TEX13D, RN7SL190P, 18 more genes
    nsv6290546copy number variation1nstd102humanPathogenic GRCh37 chrX: 119,173,583-126,584,360 , GRCh38.p12 chrX: 120,039,618-127,450,379 FBLIM1P1, PNPLA10P, 81 more genes
    nsv6138727copy number variation1nstd206human GRCh38 chrX: 124,075,000-124,218,100 , GRCh37.p13 chrX: 123,208,850-123,351,950 STAG2, HSPA8P20, 1 more genes
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