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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5958491insertion1nstd209human GRCh38 chrX: 118,352,352-118,352,352 , GRCh37.p13 chrX: 117,486,315-117,486,315 WDR44
    nsv5885826copy number variation1nstd209human GRCh38 chrX: 118,282,995-118,922,236 , GRCh37.p13 chrX: 117,416,958-118,056,199 IL13RA1, WDR44, 7 more genes
    nsv5885235copy number variation1nstd209human GRCh38 chrX: 114,977,484-119,165,869 , GRCh37.p13 chrX: 115,732,291-118,299,832 , DANT1, 52 more genes
    nsv5430321copy number variation1nstd206human GRCh38 chrX: 118,354,271-118,358,574 , GRCh37.p13 chrX: 117,488,234-117,492,537 WDR44
    nsv5429566copy number variation1nstd206human GRCh38 chrX: 118,363,414-118,363,809 , GRCh37.p13 chrX: 117,497,377-117,497,772 WDR44
    nsv5416183copy number variation1nstd206human GRCh38 chrX: 118,283,005-118,922,187 , GRCh37.p13 chrX: 117,416,968-118,056,150 IL13RA1, WDR44, 7 more genes
    nsv5414812copy number variation1nstd206human GRCh38 chrX: 118,439,203-118,441,052 , GRCh37.p13 chrX: 117,573,166-117,575,015 WDR44
    nsv5376944translocation1nstd200human GRCh38 chrX: 118,408,963-118,408,963 , GRCh38 chrX: 118,409,067-118,409,067 , GRCh37.p13 chrX: 117,542,926-117,542,926 , GRCh37.p13 chrX: 117,543,030-117,543,030 WDR44
    nsv5342907translocation1nstd200human GRCh37 chrX: 117,488,207-117,488,207 , GRCh37 chrX: 117,492,442-117,492,442 , GRCh38.p12 chrX: 118,358,479-118,358,479 , GRCh38.p12 chrX: 118,354,244-118,354,244 WDR44
    nsv5197020mobile element insertion1nstd203human GRCh38 chrX: 118,368,977-118,369,018 , GRCh37.p13 chrX: 117,502,940-117,502,981 WDR44
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4909065copy number variation1nstd200human GRCh38 chrX: 118,257,917-119,035,847 , GRCh37.p13 chrX: 117,391,880-118,169,810 WDR44, MIR1277, 9 more genes
    nsv4782279copy number variation1nstd200human GRCh37 chrX: 117,497,377-117,497,772 , GRCh38.p12 chrX: 118,363,414-118,363,809 WDR44
    nsv4780165copy number variation1nstd200human GRCh37 chrX: 117,563,364-117,564,236 , GRCh38.p12 chrX: 118,429,401-118,430,273 WDR44
    nsv4780164copy number variation1nstd200human GRCh37 chrX: 117,542,926-117,543,030 , GRCh38.p12 chrX: 118,408,963-118,409,067 WDR44
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728692copy number variation1nstd102humanPathogenic GRCh37 chrX: 117,120,780-129,850,994 , GRCh38.p12 chrX: 117,986,817-130,717,020 LOC107985709, SLC25A5, 171 more genes
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