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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 more genes
    nsv4675472copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 87,792,844-109,221,844 , GRCh38.p12 chr5: 88,497,027-109,886,143 CAST, CETN3, 202 more genes
    nsv4675441copy number variation1nstd102humanPathogenic GRCh37 chr5: 92,618,672-93,196,696 , GRCh38.p12 chr5: 93,282,966-93,860,990 NR2F1, ARB2A, 4 more genes
    nsv4591817copy number variation1nstd183human GRCh37 chr5: 92,251,395-93,046,639 , GRCh38.p12 chr5: 92,915,688-93,710,933 NR2F1, ARB2A, 7 more genes
    nsv4457026copy number variation1nstd102humanPathogenic GRCh37 chr5: 92,386,982-94,865,113 , GRCh38.p12 chr5: 93,051,276-95,529,409 POLD2P1, NR2F1-AS1, 21 more genes
    nsv4455983copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,949,118-129,317,455 , GRCh38.p12 chr5: 90,653,301-129,981,762 LOC345576, LOC107986436, 419 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
    nsv4328126inversion1nstd166human GRCh37.p13 chr5: 75,669,511-101,876,780 , GRCh38.p12 chr5: 76,373,686-102,541,076 , BHMT, 331 more genes
    nsv4321173inversion1nstd166human GRCh37.p13 chr5: 86,365,040-130,339,409 , GRCh38.p12 chr5: 87,069,223-131,003,716 , APC, 481 more genes
    nsv3924896copy number variation1nstd102humanPathogenic GRCh38 chr5: 84,603,580-111,435,081 , GRCh37 chr5: 83,899,398-110,770,779 , NCBI36 chr5: 83,935,154-110,798,678 LOC107986438, GGCTP1, 254 more genes
    nsv3923406copy number variation1nstd102humanPathogenic NCBI36 chr5: 92,959,705-93,599,283 , GRCh37 chr5: 92,933,949-93,573,527 , GRCh38 chr5: 93,598,243-94,237,822 ARB2A, POU5F2, 4 more genes
    nsv3923145copy number variation1nstd102humanUncertain significance NCBI36 chr5: 92,744,309-93,112,773 , GRCh37.p13 chr5: 92,718,553-93,087,017 , GRCh38.p12 chr5: 93,382,847-93,751,311 NR2F1, POU5F2, 4 more genes
    nsv3921368copy number variation1nstd102humanPathogenic GRCh37 chr5: 86,672,700-100,860,147 , NCBI36 chr5: 86,708,456-100,888,046 , GRCh38 chr5: 87,376,883-101,524,443 LOC107986438, MTCO1P22, 158 more genes
    nsv3921006copy number variation1nstd102humanPathogenic NCBI36 chr5: 92,554,566-112,651,391 , GRCh37 chr5: 92,528,810-112,623,492 , GRCh38 chr5: 93,193,104-113,287,795 FBXL17, GJA1P1, 204 more genes
    nsv3920768copy number variation1nstd102humanPathogenic GRCh37 chr5: 92,235,441-118,949,814 , GRCh38 chr5: 92,899,734-119,614,119 , NCBI36 chr5: 92,261,197-118,977,713 LOC102724720, LOC107986388, 292 more genes
    nsv3917856copy number variation1nstd102humanPathogenic GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153 CSNK1A1P3, POLR3G, 413 more genes
    nsv3916468copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,670,423-127,412,115 , GRCh38 chr5: 90,374,606-128,076,423 , NCBI36 chr5: 89,706,179-127,440,014 LOC105379149, LOC107986365, 406 more genes
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