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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131459insertion1nstd186human GRCh37 chr22: 37,259,658-37,259,658 , GRCh38.p12 chr22: 36,863,616-36,863,616 , GRCh38.p12 chr22|NT_187631.1: 84,410-84,410 NCF4, NCF4-AS1
    nsv5393035copy number variation1nstd186human GRCh37 chr22: 37,196,093-37,196,275 , GRCh38.p12 chr22|NT_187631.1: 20,836-21,018 , GRCh38.p12 chr22: 36,800,049-36,800,231 PVALB
    nsv4885237copy number variation1nstd200human GRCh37 chr22: 37,196,061-37,196,305 , GRCh38.p12 chr22: 36,800,017-36,800,261 , GRCh38.p12 chr22|NT_187631.1: 20,804-21,048 PVALB
    nsv4883601copy number variation1nstd200human GRCh37 chr22: 37,193,919-37,194,334 , GRCh38.p12 chr22|NT_187631.1: 18,662-19,077 , GRCh38.p12 chr22: 36,797,875-36,798,290 0
    nsv4871011copy number variation1nstd200human GRCh37 chr22: 37,244,648-37,246,525 , GRCh38.p12 chr22: 36,848,606-36,850,483 , GRCh38.p12 chr22|NT_187631.1: 69,392-71,267 NCF4-AS1
    nsv4769078insertion1nstd186human GRCh37 chr22: 37,259,656-37,259,656 , GRCh38.p12 chr22: 36,863,614-36,863,614 , GRCh38.p12 chr22|NT_187631.1: 84,408-84,408 NCF4, NCF4-AS1
    nsv4755387insertion1nstd199human GRCh37 chr22: 37,259,653-37,259,653 , GRCh38.p12 chr22: 36,863,611-36,863,611 , GRCh38.p12 chr22|NT_187631.1: 84,405-84,405 NCF4, NCF4-AS1
    nsv4747285copy number variation1nstd199human GRCh37 chr22: 37,248,877-37,248,939 , GRCh38.p12 chr22: 36,852,835-36,852,897 , GRCh38.p12 chr22|NT_187631.1: 73,633-73,695 NCF4-AS1
    nsv4739781copy number variation1nstd199human GRCh37 chr22: 37,221,234-37,221,302 , GRCh38.p12 chr22: 36,825,190-36,825,258 , GRCh38.p12 chr22|NT_187631.1: 45,977-46,045 0
    nsv4734144copy number variation1nstd199human GRCh37 chr22: 37,196,058-37,196,224 , GRCh38.p12 chr22|NT_187631.1: 20,801-20,967 , GRCh38.p12 chr22: 36,800,014-36,800,180 PVALB
    nsv4684698insertion1nstd194human GRCh38.p12 chr22: 36,863,614-36,863,614 , GRCh37 chr22: 37,259,656-37,259,656 , GRCh38.p12 chr22|NT_187631.1: 84,408-84,408 NCF4, NCF4-AS1
    nsv4506288mobile element insertion1nstd166human GRCh37.p13 chr22: 37,185,542-37,185,542 , GRCh38.p12 chr22: 36,789,498-36,789,498 , GRCh38.p12 chr22|NT_187631.1: 10,285-10,285 0
    nsv4502301mobile element insertion1nstd166human GRCh37.p13 chr22: 37,206,552-37,206,552 , GRCh38.p12 chr22: 36,810,508-36,810,508 , GRCh38.p12 chr22|NT_187631.1: 31,295-31,295 PVALB
    nsv4447478insertion1nstd175human GRCh37 chr22: 37,259,655-37,259,655 , GRCh38.p12 chr22: 36,863,613-36,863,613 , GRCh38.p12 chr22|NT_187631.1: 84,407-84,407 NCF4, NCF4-AS1
    nsv4442045copy number variation1nstd175human GRCh37 chr22: 37,196,055-37,196,221 , GRCh38.p12 chr22: 36,800,011-36,800,177 , GRCh38.p12 chr22|NT_187631.1: 20,798-20,964 PVALB
    nsv4426614copy number variation1nstd174human GRCh37 chr22: 37,196,052-37,196,221 , GRCh38.p12 chr22: 36,800,008-36,800,177 , GRCh38.p12 chr22|NT_187631.1: 20,795-20,964 PVALB
    nsv4414863copy number variation1nstd174human GRCh37 chr22: 37,195,994-37,196,521 , GRCh38.p12 chr22|NT_187631.1: 20,737-21,264 , GRCh38.p12 chr22: 36,799,950-36,800,477 PVALB
    nsv4284987copy number variation1nstd166human GRCh37.p13 chr22: 37,171,000-37,180,000 , GRCh38.p12 chr22|NT_187631.1: 1-4,743 , GRCh38.p12 chr22: 36,774,956-36,783,956 IFT27
    nsv4281733copy number variation1nstd166human GRCh37.p13 chr22: 37,241,803-37,249,707 , GRCh38.p12 chr22: 36,845,760-36,853,665 , GRCh38.p12 chr22|NT_187631.1: 66,547-74,463 NCF4-AS1
    nsv4277984copy number variation1nstd166human GRCh37.p13 chr22: 37,190,641-37,190,711 , GRCh38.p12 chr22: 36,794,597-36,794,667 , GRCh38.p12 chr22|NT_187631.1: 15,384-15,454 0
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