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Results: 1 to 20 of 105

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Number of Variants: 20

Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
esv3621784indel5estd214human GRCh37 (hg19) chr9: 130,226,642-130,226,642 , GRCh38 (hg38) chr9: 127,464,363-127,464,363 LRSAM1
esv3621785copy number variation17estd214human GRCh37 (hg19) chr9: 130,232,001-130,233,936 , GRCh38 (hg38) chr9: 127,469,722-127,471,657 LRSAM1
esv3621783mobile element insertion7estd214human GRCh37 (hg19) chr9: 130,217,915-130,217,915 , GRCh38 (hg38) chr9: 127,455,636-127,455,636 LRSAM1
nsv1067806copy number variation5nstd101humanPathogenic GRCh37 (hg19) chr9: 204,193-141,073,897 , GRCh38 (hg38) chr9: 193,412-138,179,445 , NCBI36 (hg18) chr9: 194,193-140,193,718 TRH-GTG1-9, FOXD4L2, 1001 more genes
nsv1052685copy number variation1nstd100human NCBI36 (hg18) chr9: 128,905,865-129,713,576 , GRCh37 (hg19) chr9: 129,866,044-130,673,755 , GRCh38 (hg38) chr9: 127,103,765-127,911,476 MIR2861, SH2D3C, 24 more genes
nsv1039148copy number variation1nstd100human NCBI36 (hg18) chr9: 116,087,177-129,605,569 , GRCh37 (hg19) chr9: 117,047,356-130,565,748 , GRCh38 (hg38) chr9: 114,285,076-127,803,469 SNORA70C, ASTN2-AS1, 118 more genes
nsv1037141copy number variation1nstd100human NCBI36 (hg18) chr9: 129,219,833-129,583,786 , GRCh37 (hg19) chr9: 130,180,012-130,543,965 , GRCh38 (hg38) chr9: 127,417,733-127,781,686 SH2D3C, MIR3911, 10 more genes
nsv1031485copy number variation1nstd100human NCBI36 (hg18) chr9: 199,254-140,125,458 , GRCh37 (hg19) chr9: 209,254-141,005,637 , GRCh38 (hg38) chr9: 209,254-138,111,185 TRH-GTG1-9, FOXD4L2, 1001 more genes
esv3545470copy number variation1estd215human GRCh37 (hg19) chr9: 130,232,199-130,234,047 , GRCh38 (hg38) chr9: 127,469,920-127,471,768 LRSAM1
nsv995513copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr9: 203,861-141,020,389 , GRCh38 (hg38) chr9: 203,861-138,125,937 , NCBI36 (hg18) chr9: 193,861-140,140,210 TRH-GTG1-9, FOXD4L2, 1001 more genes
nsv995466copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr9: 203,862-141,020,389 , GRCh38 (hg38) chr9: 203,862-138,125,937 , NCBI36 (hg18) chr9: 193,862-140,140,210 TRH-GTG1-9, FOXD4L2, 1001 more genes
nsv984822copy number variation1nstd92human GRCh37 (hg19) chr9: 70,512,737-141,095,050 , GRCh38 (hg38) chr9: 68,220,553-138,204,600 SNORA84, SNORA70C, 695 more genes
nsv984664complex1nstd92human GRCh37 (hg19) chr9: 99,582,000-141,095,050 SNORA70C, FAM225B, 514 more genes
nsv984603copy number variation1nstd92human GRCh37 (hg19) chr9: 46,587-141,095,050 , GRCh38 (hg38) chr9: 46,587-138,204,600 TRH-GTG1-9, FOXD4L2, 1005 more genes
esv2870818insertion1estd209human GRCh37 (hg19) chr9: 130,253,286-130,253,286 , GRCh38 (hg38) chr9: 127,491,007-127,491,007 LRSAM1
esv2870817insertion1estd209human GRCh37 (hg19) chr9: 130,243,260-130,243,260 , GRCh38 (hg38) chr9: 127,480,981-127,480,981 LRSAM1
esv2870816insertion1estd209human GRCh37 (hg19) chr9: 130,241,374-130,241,374 , GRCh38 (hg38) chr9: 127,479,095-127,479,095 LRSAM1
esv2870813insertion1estd209human GRCh37 (hg19) chr9: 130,231,899-130,231,903 , GRCh38 (hg38) chr9: 127,469,620-127,469,624 LRSAM1
esv2870810insertion1estd209human GRCh37 (hg19) chr9: 130,214,604-130,214,604 , GRCh38 (hg38) chr9: 127,452,325-127,452,325 LRSAM1
esv2870811insertion1estd209human GRCh37 (hg19) chr9: 130,215,711-130,215,711 , GRCh38 (hg38) chr9: 127,453,432-127,453,432 LRSAM1

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