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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
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4679460copy number variation1nstd189human GRCh37.p13 chr5: 110,742,798-111,062,961 , GRCh38.p12 chr5: 111,407,100-111,727,264 CAMK4, NREP, 5 more genes
    nsv4589732copy number variation1nstd183human GRCh37 chr5: 110,847,875-110,850,480 , GRCh38.p12 chr5: 111,512,177-111,514,782 LOC105369177, STARD4, 1 more genes
    nsv4484742mobile element insertion1nstd166human GRCh37.p13 chr5: 110,831,635-110,831,635 , GRCh38.p12 chr5: 111,495,937-111,495,937 STARD4, CAMK4
    nsv4456071copy number variation1nstd102humanPathogenic GRCh37 chr5: 108,304,806-121,335,239 , GRCh38.p12 chr5: 108,969,105-121,999,544 HMGN1P13, LOC101927023, 153 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
    nsv4321173inversion1nstd166human GRCh37.p13 chr5: 86,365,040-130,339,409 , GRCh38.p12 chr5: 87,069,223-131,003,716 , APC, 481 more genes
    nsv4131483copy number variation1nstd166human GRCh37.p13 chr5: 110,606,798-110,876,476 , GRCh38.p12 chr5: 111,271,100-111,540,778 STARD4, CAMK4, 2 more genes
    nsv3924205copy number variation1nstd102humanPathogenic GRCh37 chr5: 110,023,143-129,439,531 , GRCh38 chr5: 110,687,442-130,103,838 , NCBI36 chr5: 110,051,042-129,467,430 CSNK1G3, EPB41L4A-AS1, 231 more genes
    nsv3923804copy number variation1nstd102humanPathogenic GRCh37 chr5: 107,644,164-125,113,490 , NCBI36 chr5: 107,672,063-125,141,389 , GRCh38 chr5: 108,308,463-125,777,797 FABP5P6, AP3S1, 202 more genes
    nsv3923731copy number variation1nstd102humanPathogenic GRCh38 chr5: 96,454,445-114,050,905 , GRCh37 chr5: 95,790,149-113,386,602 , NCBI36 chr5: 95,815,905-113,414,501 MTATP6P2, PJA2, 166 more genes
    nsv3923639copy number variation1nstd102humanPathogenic GRCh38 chr5: 106,586,078-113,006,585 , NCBI36 chr5: 105,949,678-112,370,181 , GRCh37 chr5: 105,921,779-112,342,282 RACK1P1, LOC345576, 63 more genes
    nsv3923182copy number variation1nstd102humanUncertain significance GRCh38 chr5: 110,469,276-111,738,442 , NCBI36 chr5: 109,832,876-111,102,038 , GRCh37 chr5: 109,804,977-111,074,139 STARD4-AS1, LOC100129099, 15 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
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