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Items: 1 to 20 of 89

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3893640copy number variation1nstd102humanBenign GRCh37 chr17: 1,674,429-1,686,410 , GRCh38.p12 chr17: 1,771,135-1,783,116 SMYD4, SERPINF1
    nsv6315275copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,665,408-1,680,869 , GRCh38.p12 chr17: 1,762,114-1,777,575 SMYD4, SERPINF1
    nsv7095132copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,645,209-1,731,288 , GRCh38.p12 chr17: 1,741,915-1,827,994 SMYD4, SERPINF1, 1 more genes
    nsv3923979copy number variation1nstd102humanBenign NCBI36 chr17: 1,649,795-1,806,001 , GRCh37 chr17: 1,703,045-1,859,251 , GRCh38 chr17: 1,799,751-1,955,957 SMYD4, LOC642502, 2 more genes
    nsv6637849copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,689,217-1,856,543 , GRCh38.p12 chr17: 1,785,923-1,953,249 SMYD4, RPA1, 2 more genes
    nsv6291545copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,667,995-1,791,653 , GRCh38.p12 chr17: 1,764,701-1,888,359 SMYD4, LOC642502, 2 more genes
    nsv4457569copy number variation2nstd102humanUncertain significance GRCh37 chr17: 1,708,149-1,791,988 , GRCh38.p12 chr17: 1,804,855-1,888,694 SMYD4, LOC642502, 1 more genes
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 SMYD4, RPS4XP17, 289 more genes
    nsv3915884copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093 SMYD4, LOC105371592, 222 more genes
    nsv3922546copy number variation1nstd102humanPathogenic NCBI36 chr17: 525-5,779,421 , GRCh38 chr17: 150,732-5,935,377 , GRCh37 chr17: 525-5,838,697 SMYD4, CHRNE, 198 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SMYD4, SRR, 196 more genes
    nsv3913795copy number variation1nstd102humanPathogenic NCBI36 chr17: 43,098-5,496,266 , GRCh37 chr17: 45,835-5,555,542 , GRCh38 chr17: 193,307-5,652,222 SMYD4, BHLHA9, 194 more genes
    nsv3921779copy number variation1nstd102humanPathogenic NCBI36 chr17: 87,039-4,585,577 , GRCh38 chr17: 237,248-4,735,533 , GRCh37 chr17: 396,627-4,638,828 SMYD4, ARRB2, 146 more genes
    nsv3919819copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-4,168,935 , NCBI36 chr17: 48,539-4,115,684 , GRCh38 chr17: 198,748-4,265,640 SMYD4, LOC105371430, 125 more genes
    nsv3904699copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-3,871,323 , GRCh38.p12 chr17: 157,423-3,968,029 SMYD4, OVCA2, 120 more genes
    nsv3892866copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-3,825,428 , GRCh38.p12 chr17: 150,732-3,922,134 SMYD4, OR1P1, 120 more genes
    nsv3920266copy number variation1nstd102humanPathogenic GRCh38 chr17: 226,472-3,655,099 , NCBI36 chr17: 76,263-3,505,142 , GRCh37 chr17: 396,627-3,558,393 SMYD4, RN7SL624P, 107 more genes
    nsv3902288copy number variation1nstd102humanPathogenic GRCh37 chr17: 48,858-3,379,400 , GRCh38.p12 chr17: 199,067-3,476,106 SMYD4, GEMIN4, 100 more genes
    nsv3913766copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-3,242,868 , NCBI36 chr17: 525-3,092,912 , GRCh37 chr17: 525-3,146,162 SMYD4, LOC105371483, 90 more genes
    nsv3919726copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-3,005,626 , NCBI36 chr17: 48,539-2,952,376 , GRCh38 chr17: 198,748-3,102,332 SMYD4, RN7SL608P, 81 more genes
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