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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056369inversion1nstd229human GRCh38 chr5: 65,805,475-66,519,014 , GRCh37.p13 chr5: 65,101,302-65,814,842 SREK1, LOC105379004, 7 more genes
    nsv6777129copy number variation1nstd229human GRCh38 chr5: 65,517,434-66,063,747 , GRCh37.p13 chr5: 64,813,261-65,359,575 TRIM23, RNU6-540P, 9 more genes
    nsv6774579copy number variation1nstd229human GRCh38 chr5: 65,942,764-65,945,319 , GRCh37.p13 chr5: 65,238,592-65,241,147 ERBIN, LOC100303749
    nsv6765273copy number variation1nstd229human GRCh38 chr5: 65,460,432-65,973,179 , GRCh37.p13 chr5: 64,756,259-65,269,007 NLN, RNU6-540P, 10 more genes
    nsv6763262copy number variation1nstd229human GRCh38 chr5: 65,938,388-65,944,328 , GRCh37.p13 chr5: 65,234,216-65,240,156 LOC100303749, ERBIN
    nsv6762962copy number variation1nstd229human GRCh38 chr5: 65,929,501-65,992,900 , GRCh37.p13 chr5: 65,225,329-65,288,728 ERBIN, LOC100303749
    nsv6413816copy number variation1nstd223human GRCh38 chr5: 65,917,701-65,944,900 , GRCh37.p13 chr5: 65,213,529-65,240,728 LOC100303749, ERBIN
    nsv6401993copy number variation1nstd223human GRCh38 chr5: 65,924,801-65,951,000 , GRCh37.p13 chr5: 65,220,629-65,246,828 LOC100303749, ERBIN
    nsv6395617copy number variation1nstd223human GRCh38 chr5: 65,919,001-65,983,300 , GRCh37.p13 chr5: 65,214,829-65,279,128 ERBIN, LOC100303749
    nsv6313676copy number variation1nstd102humanPathogenic GRCh37 chr5: 64,049,692-70,306,646 , GRCh38.p12 chr5: 64,753,865-71,010,819 BCL9P1, CWC27, 105 more genes
    nsv6312114copy number variation1nstd102humanPathogenic GRCh37 chr5: 63,256,278-65,374,358 , GRCh38.p12 chr5: 63,960,451-66,078,530 RNF180, RPEP1, 23 more genes
    nsv6136128copy number variation1nstd213human GRCh37 chr5: 62,820,000-66,080,001 , GRCh38.p12 chr5: 63,524,173-66,784,173 TRIM23, HTR1A, 33 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
    nsv6135192copy number variation1nstd213human GRCh37 chr5: 63,780,000-66,290,001 , GRCh38.p12 chr5: 64,484,173-66,994,173 TRIM23, CWC27, 29 more genes
    nsv6016303copy number variation1nstd212human GRCh38 chr5: 65,942,850-65,948,480 , GRCh37.p13 chr5: 65,238,678-65,244,308 ERBIN, LOC100303749
    nsv4680929copy number variation1nstd189human GRCh37.p13 chr5: 65,061,194-65,239,387 , GRCh38.p12 chr5: 65,765,367-65,943,559 ERBIN, NLN, 1 more genes
    nsv4578696copy number variation1nstd102humanLikely pathogenic GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205 TRIM23, BTF3, 215 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
    nsv4125346copy number variation1nstd166human GRCh37.p13 chr5: 64,756,246-65,269,007 , GRCh38.p12 chr5: 65,460,419-65,973,179 CENPK, PPWD1, 10 more genes
    nsv4123374copy number variation1nstd166human GRCh37.p13 chr5: 65,236,603-65,259,813 , GRCh38.p12 chr5: 65,940,775-65,963,985 ERBIN, LOC100303749
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