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Items: 1 to 20 of 278

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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
    nsv7083678copy number variation1nstd229human GRCh38 chrX: 124,383,401-124,391,700 , GRCh37.p13 chrX: 123,517,251-123,525,550 LOC105373331, TENM1
    nsv7083676copy number variation1nstd229human GRCh38 chrX: 124,365,943-125,159,438 , GRCh37.p13 chrX: 123,499,793-124,293,287 RPS26P57, LOC105373331, 2 more genes
    nsv7083673copy number variation1nstd229human GRCh38 chrX: 124,348,917-124,431,870 , GRCh37.p13 chrX: 123,482,767-123,565,720 SH2D1A, LOC105373331, 1 more genes
    nsv7083670copy number variation1nstd229human GRCh38 chrX: 124,323,639-124,590,014 , GRCh37.p13 chrX: 123,457,489-123,723,864 TEX13D, SH2D1A, 2 more genes
    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
    nsv7048896inversion1nstd229human GRCh38 chrX: 124,356,566-124,666,581 , GRCh37.p13 chrX: 123,490,416-123,800,431 TENM1, LOC105373331, 1 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
    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
    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
    nsv6290524copy number variation1nstd102humanPathogenic GRCh37 chrX: 123,350,855-123,986,893 , GRCh38.p12 chrX: 124,217,005-124,853,044 SH2D1A, TENM1, 4 more genes
    nsv6137629copy number variation1nstd213human GRCh37 chrX: 66,030,000-152,230,001 , GRCh38.p12 chrX: 66,810,158-153,061,271 ABCB7, AGTR2, 1162 more genes
    nsv6137579copy number variation1nstd213human GRCh37 chrX: 114,940,000-134,860,001 , GRCh38.p12 chrX: 115,705,680-135,719,285 AGTR2, SLC25A5, 295 more genes
    nsv6137409copy number variation1nstd213human GRCh37 chrX: 73,710,000-151,990,001 , GRCh38.p12 chrX: 74,490,165-152,821,457 ABCB7, AGTR2, 991 more genes
    nsv6137362copy number variation1nstd213human GRCh37 chrX: 104,480,000-134,870,001 , GRCh38.p12 chrX: 105,235,316-135,719,285 AGTR2, SLC25A5, 423 more genes
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