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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
    nsv7093106copy number variation1nstd102humanPathogenic GRCh38 chr22: 37,983,647-37,983,756 , GRCh37 chr22: 38,379,654-38,379,763 SOX10, POLR2F
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7077803inversion1nstd229human GRCh38 chr22: 37,989,254-37,992,597 , GRCh37.p13 chr22: 38,385,261-38,388,604 POLR2F, MIR4534
    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
    nsv7037783copy number variation1nstd229human GRCh38 chr22: 38,030,481-38,045,381 , GRCh37.p13 chr22: 38,426,488-38,441,388 POLR2F
    nsv7030689copy number variation1nstd229human GRCh38 chr22: 38,005,032-38,025,292 , GRCh37.p13 chr22: 38,401,039-38,421,299 POLR2F
    nsv7029729copy number variation1nstd229human GRCh38 chr22: 37,960,970-37,962,813 , GRCh37.p13 chr22: 38,356,977-38,358,820 POLR2F
    nsv7027806copy number variation1nstd229human GRCh38 chr22: 37,935,988-37,967,204 , GRCh37.p13 chr22: 38,331,995-38,363,211 MIR6820, MICALL1, 2 more genes
    nsv7026194copy number variation1nstd229human GRCh38 chr22: 38,003,009-38,005,911 , GRCh37.p13 chr22: 38,399,016-38,401,918 POLR2F
    nsv7020149copy number variation1nstd229human GRCh38 chr22: 37,965,974-37,981,119 , GRCh37.p13 chr22: 38,361,981-38,377,126 POLR2F, SOX10, 1 more genes
    nsv7019837copy number variation1nstd229human GRCh38 chr22: 38,021,435-38,024,581 , GRCh37.p13 chr22: 38,417,442-38,420,588 POLR2F
    nsv6596486inversion1nstd223human GRCh38 chr22: 38,004,540-38,005,196 , GRCh37.p13 chr22: 38,400,547-38,401,203 POLR2F
    nsv6555184copy number variation1nstd223human GRCh38 chr22: 38,003,008-38,005,923 , GRCh37.p13 chr22: 38,399,015-38,401,930 POLR2F
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