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Items: 1 to 20 of 281

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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
    nsv7098585copy number variation1nstd102humanUncertain significance GRCh37 chrX: 132,730,458-133,119,476 , GRCh38.p12 chrX: 133,596,430-133,985,449 GPC3, GPC3-AS1, 2 more genes
    nsv7098343copy number variation1nstd102humanUncertain significance GRCh37 chrX: 132,670,152-133,634,107 , GRCh38.p12 chrX: 133,536,124-134,500,077 MIR19B2, PHF6, 14 more genes
    nsv7098226copy number variation1nstd102humanUncertain significance GRCh37 chrX: 132,795,748-133,119,476 , GRCh38.p12 chrX: 133,661,720-133,985,449 GPC3-AS1, RPSAP63, 2 more genes
    nsv7084053copy number variation1nstd229human GRCh38 chrX: 133,869,401-133,896,400 , GRCh37.p13 chrX: 133,003,428-133,030,427 GPC3-AS1, GPC3
    nsv7084046copy number variation1nstd229human GRCh38 chrX: 133,802,954-134,275,795 , GRCh37.p13 chrX: 132,936,981-133,409,825 MIR363, NT5DC1P2, 10 more genes
    nsv7054310inversion1nstd229human GRCh38 chrX: 133,816,786-134,069,258 , GRCh37.p13 chrX: 132,950,813-133,203,287 GPC3-AS1, GPC3
    nsv7042777inversion1nstd229human GRCh38 chrX: 127,009,007-134,341,039 , GRCh37.p13 chrX: 126,142,990-133,475,069 ELF4, TJAP1P1, 97 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
    nsv6634474delins1nstd102humanPathogenic GRCh37 chrX: 133,030,929-133,079,463 , GRCh38.p12 chrX: 133,896,902-133,945,436 GPC3, GPC3-AS1
    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
    nsv6313035copy number variation1nstd102humanPathogenic GRCh37 chrX: 132,670,132-133,119,496 , GRCh38.p12 chrX: 133,536,104-133,985,469 GPC3, GPC3-AS1, 2 more genes
    nsv6291799copy number variation1nstd102humanPathogenic GRCh38 chrX: 133,658,037-133,915,611 , GRCh37.p13 chrX: 132,792,065-133,049,638 GPC3, RPS24P19, 2 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
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