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Items: 1 to 20 of 311

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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
    nsv7083783copy number variation1nstd229human GRCh38 chrX: 131,277,221-131,342,603 , GRCh37.p13 chrX: 130,411,195-130,476,577 OR5AW1P, OR11N1P, 1 more genes
    nsv7083782copy number variation1nstd229human GRCh38 chrX: 131,265,187-131,279,535 , GRCh37.p13 chrX: 130,399,161-130,413,509 IGSF1
    nsv7083775copy number variation1nstd229human GRCh38 chrX: 131,154,720-131,587,042 , GRCh37.p13 chrX: 130,288,694-130,721,016 LOC102723546, OR11N1P, 10 more genes
    nsv7083774copy number variation1nstd229human GRCh38 chrX: 131,154,701-131,587,000 , GRCh37.p13 chrX: 130,288,675-130,720,974 OR5BH1P, LOC107985705, 10 more genes
    nsv7083765copy number variation1nstd229human GRCh38 chrX: 131,052,776-131,955,850 , GRCh37.p13 chrX: 130,186,750-131,089,878 LOC100421910, RNA5SP514, 20 more genes
    nsv7083764copy number variation1nstd229human GRCh38 chrX: 131,020,434-131,759,328 , GRCh37.p13 chrX: 130,154,408-130,893,356 FIRRE, NLRP7P1, 17 more genes
    nsv7057758inversion1nstd229human GRCh38 chrX: 131,288,310-131,632,567 , GRCh37.p13 chrX: 130,422,284-130,766,569 OR7L1P, OR5AW1P, 11 more genes
    nsv7056871inversion1nstd229human GRCh38 chrX: 130,673,493-132,574,143 , GRCh37.p13 chrX: 129,807,467-131,708,171 OR1AA1P, RNA5SP514, 28 more genes
    nsv7050206inversion1nstd229human GRCh38 chrX: 130,371,007-132,177,030 , GRCh37.p13 chrX: 129,504,981-131,311,058 FSIP2LP, SLC25A14, 32 more genes
    nsv7048567inversion1nstd229human GRCh38 chrX: 130,911,451-132,582,679 , GRCh37.p13 chrX: 130,045,425-131,716,707 RAP2C-AS1, FIRRE, 27 more genes
    nsv7042777inversion1nstd229human GRCh38 chrX: 127,009,007-134,341,039 , GRCh37.p13 chrX: 126,142,990-133,475,069 ELF4, TJAP1P1, 97 more genes
    nsv7041789inversion1nstd229human GRCh38 chrX: 131,096,788-131,683,848 , GRCh37.p13 chrX: 130,230,762-130,817,881 LOC107985705, OR2AF1P, 14 more genes
    nsv7041211inversion1nstd229human GRCh38 chrX: 131,132,088-132,749,775 , GRCh37.p13 chrX: 130,266,062-131,883,803 RN7SL191P, OR7L1P, 27 more genes
    nsv6636407copy number variation1nstd102humanPathogenic GRCh37 chrX: 124,749,464-155,233,731 , GRCh38.p12 chrX: 125,615,468-156,004,066 RN7SKP31, LOC728470, 539 more genes
    nsv6634389copy number variation1nstd102humanPathogenic GRCh37 chrX: 129,711,889-132,794,615 , GRCh38.p12 chrX: 130,577,915-133,660,587 LOC107985705, OR11Q1P, 40 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6633819copy number variation1nstd224human GRCh37 chrX: 129,518,496-130,450,360 , GRCh38.p12 chrX: 130,384,522-131,316,386 IGSF1, GPR119, 11 more genes
    nsv6633770copy number variation1nstd224human GRCh37 chrX: 130,413,979-130,483,078 , GRCh38.p12 chrX: 131,280,005-131,349,104 IGSF1, OR5AW1P, 1 more genes
    nsv6633769copy number variation1nstd224human GRCh37 chrX: 130,178,395-131,122,443 , GRCh38.p12 chrX: 131,044,421-131,988,415 IGSF1, OR1AA1P, 20 more genes
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