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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7140831insertion1nstd232human GRCh37.p13 chr4: 42,051,497-42,051,497 , GRCh38.p12 chr4: 42,049,480-42,049,480 SLC30A9
    nsv7054319inversion1nstd229human GRCh38 chr4: 40,437,339-43,087,585 , GRCh37.p13 chr4: 40,439,356-43,089,602 RN7SKP82, RPS7P7, 33 more genes
    nsv6734569copy number variation1nstd229human GRCh38 chr4: 41,989,401-42,049,700 , GRCh37.p13 chr4: 41,991,418-42,051,717 SLC30A9, ATP1B1P1
    nsv6732348copy number variation1nstd229human GRCh38 chr4: 42,021,918-42,022,102 , GRCh37.p13 chr4: 42,023,935-42,024,119 SLC30A9
    nsv6730348copy number variation1nstd229human GRCh38 chr4: 42,081,988-42,088,316 , GRCh37.p13 chr4: 42,084,005-42,090,333 SLC30A9
    nsv6730097copy number variation1nstd229human GRCh38 chr4: 42,083,874-42,087,388 , GRCh37.p13 chr4: 42,085,891-42,089,405 SLC30A9
    nsv6729588copy number variation1nstd229human GRCh38 chr4: 41,990,101-41,991,400 , GRCh37.p13 chr4: 41,992,118-41,993,417 SLC30A9
    nsv6725416copy number variation1nstd229human GRCh38 chr4: 42,018,502-42,018,541 , GRCh37.p13 chr4: 42,020,519-42,020,558 SLC30A9
    nsv6724662copy number variation1nstd229human GRCh38 chr4: 41,994,990-41,997,565 , GRCh37.p13 chr4: 41,997,007-41,999,582 SLC30A9
    nsv6723935copy number variation1nstd229human GRCh38 chr4: 42,063,973-42,067,652 , GRCh37.p13 chr4: 42,065,990-42,069,669 SLC30A9
    nsv6722609copy number variation1nstd229human GRCh38 chr4: 42,084,462-42,084,802 , GRCh37.p13 chr4: 42,086,479-42,086,819 SLC30A9
    nsv6721704copy number variation1nstd229human GRCh38 chr4: 42,018,001-42,021,500 , GRCh37.p13 chr4: 42,020,018-42,023,517 SLC30A9
    nsv6721153copy number variation1nstd229human GRCh38 chr4: 42,052,001-42,063,200 , GRCh37.p13 chr4: 42,054,018-42,065,217 SLC30A9
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6571489inversion1nstd223human GRCh38 chr4: 41,996,151-41,997,013 , GRCh37.p13 chr4: 41,998,168-41,999,030 SLC30A9
    nsv6571313inversion1nstd223human GRCh38 chr4: 42,082,117-42,084,460 , GRCh37.p13 chr4: 42,084,134-42,086,477 SLC30A9
    nsv6569133inversion1nstd223human GRCh38 chr4: 42,090,741-42,091,503 , GRCh37.p13 chr4: 42,092,758-42,093,520 SLC30A9
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