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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096310copy number variation1nstd102humanPathogenic GRCh37 chr22: 38,097,373-39,306,081 , GRCh38.p12 chr22: 37,701,366-38,910,076 TMEM184B, ANKRD54, 46 more genes
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7095836copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr22: 37,154,355-39,148,633 , GRCh38.p12 chr22: 36,758,311-38,752,628 CSF2RBP1, H1-0, 80 more genes
    nsv7077764inversion1nstd229human GRCh38 chr22: 37,971,370-41,589,449 , GRCh37.p13 chr22: 38,367,377-41,985,453 UQCRFS1P1, LOC105373027, 119 more genes
    nsv7072766inversion1nstd229human GRCh38 chr22: 35,603,617-39,341,195 , GRCh37.p13 chr22: 35,999,664-39,737,200 APOL5, MTATP6P20, 132 more genes
    nsv7064066inversion1nstd229human GRCh38 chr22: 34,920,312-39,418,308 , GRCh37.p13 chr22: 35,316,302-39,814,313 LOC112268295, APOBEC3B-AS1, 150 more genes
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7059210inversion1nstd229human GRCh38 chr22: 35,603,611-39,337,136 , GRCh37.p13 chr22: 35,999,658-39,733,141 MTCO2P20, RPS29P31, 132 more genes
    nsv7028577copy number variation1nstd229human GRCh38 chr22: 38,690,744-38,706,805 , GRCh37.p13 chr22: 39,086,749-39,102,810 JOSD1, GTPBP1
    nsv7025777copy number variation1nstd229human GRCh38 chr22: 38,695,738-38,698,920 , GRCh37.p13 chr22: 39,091,743-39,094,925 JOSD1
    nsv7024459copy number variation1nstd229human GRCh38 chr22: 38,696,754-38,699,688 , GRCh37.p13 chr22: 39,092,759-39,095,693 JOSD1
    nsv6553262copy number variation1nstd223human GRCh38 chr22: 38,698,165-38,698,549 , GRCh37.p13 chr22: 39,094,170-39,094,554 JOSD1
    nsv6550822copy number variation1nstd223human GRCh38 chr22: 38,690,744-38,706,804 , GRCh37.p13 chr22: 39,086,749-39,102,809 GTPBP1, JOSD1
    nsv6546511copy number variation1nstd223human GRCh38 chr22: 38,696,754-38,699,685 , GRCh37.p13 chr22: 39,092,759-39,095,690 JOSD1
    nsv6546014copy number variation1nstd223human GRCh38 chr22: 38,685,756-38,691,122 , GRCh37.p13 chr22: 39,081,761-39,087,127 TOMM22, JOSD1
    nsv6134588copy number variation1nstd213human GRCh37 chr22: 38,630,000-39,360,001 , GRCh38.p12 chr22: 38,233,994-38,963,996 CSNK1E, KCNJ4, 24 more genes
    nsv6134213copy number variation1nstd213human GRCh37 chr22: 37,470,000-39,980,001 , GRCh38.p12 chr22: 37,073,960-39,583,996 ATF4, COX5BP7, 98 more genes
    nsv6134212copy number variation1nstd213human GRCh37 chr22: 36,430,000-39,960,001 , GRCh38.p12 chr22: 36,033,952-39,563,996 ATF4, COX5BP7, 133 more genes
    nsv5197210mobile element insertion1nstd203human GRCh38 chr22: 38,684,939-38,684,961 , GRCh37.p13 chr22: 39,080,944-39,080,966 TOMM22, JOSD1
    nsv5040141copy number variation1nstd200human GRCh38 chr22: 38,690,744-38,706,805 , GRCh37.p13 chr22: 39,086,749-39,102,810 GTPBP1, JOSD1
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