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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5892948copy number variation1nstd209human GRCh38 chr5: 63,643,600-63,684,630 , GRCh37.p13 chr5: 62,939,427-62,980,457 LOC107986416
    nsv5308551copy number variation1nstd204human GRCh38.p13 chr5: 63,281,489-63,875,171 , GRCh37.p13 chr5: 62,577,316-63,170,998 , LOC100420027, 1 more genes
    nsv5236590copy number variation1nstd204human GRCh38.p13 chr5: 63,689,575-63,716,106 , GRCh37.p13 chr5: 62,985,402-63,011,933 LOC107986416
    nsv5236584copy number variation1nstd204human GRCh38.p13 chr5: 63,281,301-63,875,100 , GRCh37.p13 chr5: 62,577,128-63,170,927 , LOC100420027, 1 more genes
    nsv4948832copy number variation1nstd200human GRCh38 chr5: 63,281,499-63,875,169 , GRCh37.p13 chr5: 62,577,326-63,170,996 , LOC100420027, 1 more genes
    nsv4937546copy number variation1nstd200human GRCh38 chr5: 63,643,606-63,684,631 , GRCh37.p13 chr5: 62,939,433-62,980,458 LOC107986416
    nsv4805556copy number variation1nstd200human GRCh37 chr5: 62,577,326-63,170,996 , GRCh38.p12 chr5: 63,281,499-63,875,169 , LOC107986416, 1 more genes
    nsv4803251copy number variation1nstd200human GRCh37 chr5: 62,939,433-62,980,458 , GRCh38.p12 chr5: 63,643,606-63,684,631 LOC107986416
    nsv4591493copy number variation1nstd183human GRCh37 chr5: 62,903,005-62,989,170 , GRCh38.p12 chr5: 63,607,178-63,693,343 LOC107986416
    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
    nsv4521974copy number variation1nstd166human GRCh37.p13 chr5: 62,877,999-63,488,200 , GRCh38.p12 chr5: 63,582,172-64,192,373 LOC107986416, RNF180, 2 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
    nsv4401983copy number variation1nstd174human GRCh37 chr5: 62,895,028-62,990,697 , GRCh38.p12 chr5: 63,599,201-63,694,870 LOC107986416
    nsv4337631sequence alteration1nstd166human GRCh37.p13 chr5: 59,960,463-64,048,177 , GRCh38.p12 chr5: 60,664,636-64,752,350 , ERCC8, 46 more genes
    nsv4131633copy number variation1nstd166human GRCh37.p13 chr5: 62,527,405-63,960,327 , GRCh38.p12 chr5: 63,231,578-64,664,500 , HTR1A, 7 more genes
    nsv4119813copy number variation1nstd166human GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790 , ESM1, 305 more genes
    nsv4115055copy number variation1nstd166human GRCh37.p13 chr5: 62,597,103-63,181,549 , GRCh38.p12 chr5: 63,301,276-63,885,722 , LOC107986416, 2 more genes
    nsv3962831insertion1nstd168human GRCh38 chr5: 63,689,422-63,725,765 , GRCh37.p13 chr5: 62,985,249-63,021,592 LOC107986416
    nsv3920421copy number variation1nstd102humanLikely pathogenic NCBI36 chr5: 62,538,695-70,622,774 , GRCh37 chr5: 62,502,939-70,587,018 , GRCh38 chr5: 63,207,112-71,291,191 TRIM23, CCNB1, 124 more genes
    nsv3919086copy number variation1nstd102humanPathogenic NCBI36 chr5: 59,830,661-63,259,366 , GRCh38 chr5: 60,499,077-63,927,783 , GRCh37 chr5: 59,794,904-63,223,610 LOC105378999, DEPDC1B, 40 more genes
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