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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142411copy number variation1nstd232human GRCh37.p13 chr22: 41,751,866-41,751,956 , GRCh38.p12 chr22: 41,355,862-41,355,952 ZC3H7B
    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
    nsv7071135inversion1nstd229human GRCh38 chr22: 41,311,089-41,312,014 , GRCh37.p13 chr22: 41,707,093-41,708,018 ZC3H7B
    nsv7069304inversion1nstd229human GRCh38 chr22: 41,294,727-42,750,704 , GRCh37.p13 chr22: 41,690,731-43,146,710 SERHL2, CSDC2, 63 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
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7058630inversion1nstd229human GRCh38 chr22: 41,311,167-41,315,607 , GRCh37.p13 chr22: 41,707,171-41,711,611 ZC3H7B
    nsv7037110copy number variation1nstd229human GRCh38 chr22: 41,312,169-41,314,925 , GRCh37.p13 chr22: 41,708,173-41,710,929 ZC3H7B
    nsv7034513copy number variation1nstd229human GRCh38 chr22: 41,333,497-41,336,716 , GRCh37.p13 chr22: 41,729,501-41,732,720 ZC3H7B
    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
    nsv7022955copy number variation1nstd229human GRCh38 chr22: 41,175,146-41,333,607 , GRCh37.p13 chr22: 41,571,150-41,729,611 EP300, MIR6889, 8 more genes
    nsv7018662copy number variation1nstd229human GRCh38 chr22: 41,360,479-41,362,932 , GRCh37.p13 chr22: 41,756,483-41,758,936 ZC3H7B
    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
    nsv6596540inversion1nstd223human GRCh38 chr22: 41,311,180-41,315,605 , GRCh37.p13 chr22: 41,707,184-41,711,609 ZC3H7B
    nsv6596534inversion1nstd223human GRCh38 chr22: 39,133,553-42,757,193 , GRCh37.p13 chr22: 39,529,558-43,153,199 POLR3H, ACO2, 123 more genes
    nsv6554968copy number variation1nstd223human GRCh38 chr22: 41,303,856-41,306,408 , GRCh37.p13 chr22: 41,699,860-41,702,412 ZC3H7B
    nsv6550997copy number variation1nstd223human GRCh38 chr22: 41,312,173-41,314,925 , GRCh37.p13 chr22: 41,708,177-41,710,929 ZC3H7B
    nsv6548417copy number variation1nstd223human GRCh38 chr22: 41,303,816-41,309,325 , GRCh37.p13 chr22: 41,699,820-41,705,329 ZC3H7B
    nsv6545517copy number variation1nstd223human GRCh38 chr22: 41,360,479-41,362,929 , GRCh37.p13 chr22: 41,756,483-41,758,933 ZC3H7B
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