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Items: 1 to 20 of 46

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6311712copy number variation1nstd102humanPathogenic GRCh37 chr4: 129,857,790-129,869,745 , GRCh38.p12 chr4: 128,936,635-128,948,590 SCLT1
    nsv6311822copy number variation1nstd102humanPathogenic GRCh37 chr4: 129,960,176-129,965,226 , GRCh38.p12 chr4: 129,039,021-129,044,071 SCLT1
    nsv7096833copy number variation1nstd102humanPathogenic GRCh37 chr4: 130,003,441-130,003,548 , GRCh38.p12 chr4: 129,082,286-129,082,393 SCLT1
    nsv6311902copy number variation1nstd102humanUncertain significance GRCh37 chr4: 129,886,362-129,891,643 , GRCh38.p12 chr4: 128,965,207-128,970,488 SCLT1
    nsv6311821copy number variation1nstd102humanUncertain significance GRCh37 chr4: 129,805,632-129,925,051 , GRCh38.p12 chr4: 128,884,477-129,003,896 SCLT1
    nsv6312236copy number variation1nstd102humanUncertain significance GRCh37 chr4: 129,864,131-129,920,969 , GRCh38.p12 chr4: 128,942,976-128,999,814 SCLT1
    nsv6311903copy number variation1nstd102humanPathogenic GRCh37 chr4: 129,960,176-130,014,258 , GRCh38.p12 chr4: 129,039,021-129,093,103 SCLT1, C4orf33
    nsv3888470copy number variation1nstd102humanBenign GRCh37 chr4: 129,773,881-129,939,775 , GRCh38.p12 chr4: 128,852,726-129,018,620 SCLT1, JADE1
    nsv3889170copy number variation1nstd102humanBenign GRCh37 chr4: 129,773,881-129,927,804 , GRCh38.p12 chr4: 128,852,726-129,006,649 SCLT1, JADE1
    nsv3923485copy number variation1nstd102humanBenign/Likely benign NCBI36 chr4: 129,997,476-130,124,506 , GRCh37 chr4: 129,778,026-129,905,056 , GRCh38 chr4: 128,856,871-128,983,901 SCLT1, JADE1
    nsv3918217copy number variation1nstd102humanBenign NCBI36 chr4: 130,005,133-130,077,442 , GRCh37 chr4: 129,785,683-129,857,992 , GRCh38 chr4: 128,864,528-128,936,837 SCLT1, JADE1
    nsv3910163copy number variation1nstd102humanUncertain significance NCBI36 chr4: 129,977,655-130,158,811 , GRCh37.p13 chr4: 129,758,205-129,939,361 , GRCh38.p12 chr4: 128,837,050-129,018,206 SCLT1, JADE1
    nsv3882653copy number variation1nstd102humannot provided GRCh38 chr4: 128,853,220-129,006,649 , GRCh37 chr4: 129,774,375-129,927,804 SCLT1, JADE1
    esv3648198copy number variation1estd216humannot provided GRCh38.p12 chr4: 128,853,220-129,006,649 , GRCh37 chr4: 129,774,375-129,927,804 SCLT1, JADE1
    nsv6290862copy number variation1nstd102humanUncertain significance GRCh37 chr4: 129,938,155-130,059,879 , GRCh38.p12 chr4: 129,017,000-129,138,724 SCLT1, ZSWIM5P3, 2 more genes
    nsv3917126copy number variation1nstd102humanPathogenic GRCh38 chr4: 116,630,862-145,429,900 , NCBI36 chr4: 117,771,466-146,570,502 , GRCh37 chr4: 117,552,018-146,351,052 SCLT1, SETD7, 294 more genes
    nsv6290265copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113 SCLT1, LOC105379404, 218 more genes
    nsv3922957copy number variation1nstd102humanPathogenic GRCh37 chr4: 118,273,037-134,486,822 , GRCh38 chr4: 117,351,881-133,565,667 , NCBI36 chr4: 118,492,485-134,706,272 SCLT1, LOC102724158, 168 more genes
    nsv3874323copy number variation1nstd102humanPathogenic GRCh37 chr4: 126,549,693-141,313,049 , GRCh38.p12 chr4: 125,628,538-140,391,895 SCLT1, FTH1P24, 127 more genes
    nsv3912421copy number variation1nstd102humanPathogenic NCBI36 chr4: 129,260,477-143,571,978 , GRCh37 chr4: 129,041,027-143,352,528 , GRCh38 chr4: 128,119,872-142,431,375 SCLT1, PCDH10-DT, 120 more genes
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