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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5472652copy number variation1nstd206human GRCh38 chr5: 34,558,065-35,071,637 , GRCh37.p13 chr5: 34,558,170-35,071,739 AGXT2, RAI14, 9 more genes
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5469056copy number variation1nstd206human GRCh38 chr5: 34,921,369-34,943,155 , GRCh37.p13 chr5: 34,921,474-34,943,260 DNAJC21, BRIX1
    nsv5460316copy number variation1nstd206human GRCh38 chr5: 34,948,267-34,948,432 , GRCh37.p13 chr5: 34,948,372-34,948,537 DNAJC21
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv4944591copy number variation1nstd200human GRCh38 chr5: 34,921,629-34,942,935 , GRCh37.p13 chr5: 34,921,734-34,943,040 BRIX1, DNAJC21
    nsv4937298copy number variation1nstd200human GRCh38 chr5: 34,956,496-34,964,996 , GRCh37.p13 chr5: 34,956,601-34,965,101 DNAJC21
    nsv4805390copy number variation1nstd200human GRCh37 chr5: 34,921,725-34,943,046 , GRCh38.p12 chr5: 34,921,620-34,942,941 DNAJC21, BRIX1
    nsv4701795copy number variation1nstd195human GRCh37 chr5: 34,922,101-34,941,451 , GRCh38.p12 chr5: 34,921,996-34,941,346 BRIX1, DNAJC21
    nsv4598080copy number variation1nstd183human GRCh37 chr5: 34,798,601-34,983,158 , GRCh38.p12 chr5: 34,798,496-34,983,053 RAD1, RAI14, 5 more genes
    nsv4593083copy number variation1nstd183human GRCh37 chr5: 34,929,085-34,930,121 , GRCh38.p12 chr5: 34,928,980-34,930,016 DNAJC21
    nsv4456866copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,453,883-46,389,339 , GRCh38.p12 chr5: 34,453,778-46,389,237 LOC100506639, EEF1A1P19, 146 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4406140copy number variation1nstd174human GRCh37 chr5: 34,934,772-35,064,147 , GRCh38.p12 chr5: 34,934,667-35,064,045 PRLR, AGXT2, 1 more genes
    nsv4375946copy number variation1nstd173human GRCh37 chr5: 34,796,144-34,986,042 , GRCh38.p12 chr5: 34,796,039-34,985,937 RAI14, TTC23L, 5 more genes
    nsv4337099sequence alteration1nstd166human GRCh37.p13 chr5: 34,227,063-35,061,161 , GRCh38.p12 chr5: 34,226,958-35,061,059 RAD1, DNAJC21, 12 more genes
    nsv4131353copy number variation1nstd166human GRCh37.p13 chr5: 34,938,484-34,938,539 , GRCh38.p12 chr5: 34,938,379-34,938,434 DNAJC21
    nsv4128648copy number variation1nstd166human GRCh37.p13 chr5: 34,921,784-34,942,978 , GRCh38.p12 chr5: 34,921,679-34,942,873 BRIX1, DNAJC21
    nsv4123973copy number variation1nstd166human GRCh37.p13 chr5: 34,929,785-34,929,840 , GRCh38.p12 chr5: 34,929,680-34,929,735 DNAJC21
    nsv4116196copy number variation1nstd166human GRCh37.p13 chr5: 34,939,270-34,939,448 , GRCh38.p12 chr5: 34,939,165-34,939,343 DNAJC21
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