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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7056711inversion1nstd229human GRCh38 chr4: 48,114,954-48,115,001 , GRCh37.p13 chr4: 48,116,971-48,117,018 TXK
    nsv7048273inversion1nstd229human GRCh38 chr4: 48,084,181-48,084,214 , GRCh37.p13 chr4: 48,086,198-48,086,231 TXK
    nsv6736919copy number variation1nstd229human GRCh38 chr4: 48,092,553-48,092,620 , GRCh37.p13 chr4: 48,094,570-48,094,637 TXK
    nsv6736827copy number variation1nstd229human GRCh38 chr4: 48,075,645-48,075,711 , GRCh37.p13 chr4: 48,077,662-48,077,728 TXK
    nsv6735800copy number variation1nstd229human GRCh38 chr4: 48,058,936-48,064,412 , GRCh37.p13 chr4: 48,060,953-48,066,429 TXK
    nsv6731421copy number variation1nstd229human GRCh38 chr4: 48,129,771-48,135,015 , GRCh37.p13 chr4: 48,131,788-48,137,032 TXK, TEC
    nsv6731278copy number variation1nstd229human GRCh38 chr4: 48,107,447-48,122,274 , GRCh37.p13 chr4: 48,109,464-48,124,291 TXK
    nsv6729527copy number variation1nstd229human GRCh38 chr4: 48,099,678-48,104,585 , GRCh37.p13 chr4: 48,101,695-48,106,602 TXK, RNU6-838P
    nsv6729436copy number variation1nstd229human GRCh38 chr4: 48,112,741-48,121,318 , GRCh37.p13 chr4: 48,114,758-48,123,335 TXK
    nsv6728582copy number variation1nstd229human GRCh38 chr4: 48,117,442-48,124,335 , GRCh37.p13 chr4: 48,119,459-48,126,352 TXK
    nsv6727880copy number variation1nstd229human GRCh38 chr4: 48,110,191-48,112,952 , GRCh37.p13 chr4: 48,112,208-48,114,969 TXK
    nsv6725685copy number variation1nstd229human GRCh38 chr4: 48,097,714-48,102,227 , GRCh37.p13 chr4: 48,099,731-48,104,244 TXK
    nsv6724809copy number variation1nstd229human GRCh38 chr4: 48,124,442-48,129,730 , GRCh37.p13 chr4: 48,126,459-48,131,747 TXK
    nsv6721576copy number variation1nstd229human GRCh38 chr4: 48,064,260-48,067,833 , GRCh37.p13 chr4: 48,066,277-48,069,850 TXK
    nsv6721281copy number variation1nstd229human GRCh38 chr4: 48,068,901-48,073,100 , GRCh37.p13 chr4: 48,070,918-48,075,117 TXK
    nsv6720663copy number variation1nstd229human GRCh38 chr4: 48,068,913-48,069,050 , GRCh37.p13 chr4: 48,070,930-48,071,067 TXK
    nsv6718642copy number variation1nstd229human GRCh38 chr4: 48,106,784-48,108,890 , GRCh37.p13 chr4: 48,108,801-48,110,907 TXK
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
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