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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906880copy number variation1nstd209human GRCh38 chr4: 118,322,558-118,325,921 , GRCh37.p13 chr4: 119,243,713-119,247,076 PRSS12
    nsv5837860copy number variation1nstd209human GRCh38 chr4: 118,322,666-118,325,975 , GRCh37.p13 chr4: 119,243,821-119,247,130 PRSS12
    nsv5685716mobile element insertion1nstd211human GRCh38 chr4: 118,326,524-118,326,524 , GRCh37.p13 chr4: 119,247,679-119,247,679 PRSS12
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5454405copy number variation1nstd206human GRCh38 chr4: 118,322,561-118,325,922 , GRCh37.p13 chr4: 119,243,716-119,247,077 PRSS12
    nsv5400487mobile element insertion1nstd206human GRCh38 chr4: 118,326,524-118,326,575 , GRCh37.p13 chr4: 119,247,679-119,247,730 PRSS12
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5317762copy number variation1nstd204human GRCh38.p13 chr4: 118,322,561-118,325,922 , GRCh37.p13 chr4: 119,243,716-119,247,077 PRSS12
    nsv5227738copy number variation1nstd204human GRCh38.p13 chr4: 118,322,566-118,325,975 , GRCh37.p13 chr4: 119,243,721-119,247,130 PRSS12
    nsv5223699copy number variation1nstd204human GRCh38.p13 chr4: 118,302,901-118,308,100 , GRCh37.p13 chr4: 119,224,056-119,229,255 PRSS12
    nsv4943903copy number variation1nstd200human GRCh38 chr4: 118,193,133-118,653,407 , GRCh37.p13 chr4: 119,114,288-119,574,562 SNORA24, LOC729218, 11 more genes
    nsv4935525copy number variation1nstd200human GRCh38 chr4: 118,339,534-118,341,727 , GRCh37.p13 chr4: 119,260,689-119,262,882 PRSS12
    nsv4935524copy number variation1nstd200human GRCh38 chr4: 118,322,561-118,325,922 , GRCh37.p13 chr4: 119,243,716-119,247,077 PRSS12
    nsv4808176copy number variation1nstd200human GRCh37 chr4: 119,243,716-119,247,077 , GRCh38.p12 chr4: 118,322,561-118,325,922 PRSS12
    nsv4808175copy number variation1nstd200human GRCh37 chr4: 119,235,902-119,236,226 , GRCh38.p12 chr4: 118,314,747-118,315,071 PRSS12
    nsv4808174copy number variation1nstd200human GRCh37 chr4: 119,231,811-119,232,111 , GRCh38.p12 chr4: 118,310,656-118,310,956 PRSS12
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
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