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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139937copy number variation1nstd232human GRCh37.p13 chr22: 39,917,675-39,917,775 , GRCh38.p12 chr22: 39,521,670-39,521,770 ATF4
    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
    nsv7077764inversion1nstd229human GRCh38 chr22: 37,971,370-41,589,449 , GRCh37.p13 chr22: 38,367,377-41,985,453 UQCRFS1P1, LOC105373027, 119 more genes
    nsv7072452inversion1nstd229human GRCh38 chr22: 39,519,735-39,519,852 , GRCh37.p13 chr22: 39,915,740-39,915,857 ATF4
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7029088copy number variation1nstd229human GRCh38 chr22: 39,523,058-39,523,093 , GRCh37.p13 chr22: 39,919,063-39,919,098 ATF4
    nsv7028404copy number variation1nstd229human GRCh38 chr22: 39,519,401-39,521,100 , GRCh37.p13 chr22: 39,915,406-39,917,105 ATF4
    nsv7027972copy number variation1nstd229human GRCh38 chr22: 39,501,395-39,515,332 , GRCh37.p13 chr22: 39,897,400-39,911,337 LOC105373035, ATF4, 1 more genes
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv7020429copy number variation1nstd229human GRCh38 chr22: 39,407,096-39,566,174 , GRCh37.p13 chr22: 39,803,101-39,962,179 MGAT3-AS1, RPS19BP1, 6 more genes
    nsv6637214copy number variation1nstd102humanUncertain significance GRCh37 chr22: 39,768,795-41,946,225 , GRCh38.p12 chr22: 39,372,790-41,550,221 MRTFA-AS1, LOC105373043, 62 more genes
    nsv6626954copy number variation1nstd224human GRCh37 chr22: 39,907,318-40,563,020 , GRCh38.p12 chr22: 39,511,313-40,167,016 ATF4, MIEF1, 12 more genes
    nsv6596534inversion1nstd223human GRCh38 chr22: 39,133,553-42,757,193 , GRCh37.p13 chr22: 39,529,558-43,153,199 POLR3H, ACO2, 123 more genes
    nsv6311136copy number variation1nstd102humanUncertain significance GRCh37 chr22: 39,621,728-41,077,932 , GRCh38.p12 chr22: 39,225,723-40,681,928 TAB1, TNRC6B, 34 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
    nsv5360582translocation1nstd200human GRCh38 chr22: 39,521,241-39,521,241 , GRCh38 chr22: 39,521,136-39,521,136 , GRCh37.p13 chr22: 39,917,141-39,917,141 , GRCh37.p13 chr22: 39,917,246-39,917,246 ATF4
    nsv5333790translocation1nstd200human GRCh37 chr22: 39,917,246-39,917,246 , GRCh37 chr22: 39,917,141-39,917,141 , GRCh38.p12 chr22: 39,521,136-39,521,136 , GRCh38.p12 chr22: 39,521,241-39,521,241 ATF4
    nsv5288097copy number variation1nstd204human GRCh38.p13 chr22: 38,982,101-39,534,900 , GRCh37.p13 chr22: 39,378,106-39,930,905 APOBEC3C, COX5BP7, 25 more genes
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