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Results: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1357682copy number variation1nstd122human NCBI36 (hg18) chr9: 129,073,303-129,074,524 , GRCh37 (hg19) chr9: 130,033,482-130,034,703 , GRCh38 (hg38) chr9: 127,271,203-127,272,424 GARNL3
    nsv1194854copy number variation2nstd113human NCBI36 (hg18) chr9: 128,995,143-129,151,685 , GRCh37 (hg19) chr9: 129,955,322-130,111,864 , GRCh38 (hg38) chr9: 127,193,043-127,349,585 GARNL3, RALGPS1
    nsv1189447copy number variation1nstd113human NCBI36 (hg18) chr9: 128,807,165-138,399,135 , GRCh37 (hg19) chr9: 129,767,344-139,279,314 , GRCh38 (hg38) chr9: 127,005,065-136,384,862 LINC01502, RNU6ATAC, 195 more genes
    nsv1188337copy number variation1nstd113human 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
    nsv1147209insertion1nstd107human GRCh37 (hg19) chr9: 130,006,694-130,006,769 , GRCh38 (hg38) chr9: 127,244,415-127,244,490 GARNL3
    nsv1113017copy number variation1nstd106human GRCh37 (hg19) chr9: 129,987,200-129,987,700 , GRCh38 (hg38) chr9: 127,224,921-127,225,421 GARNL3
    nsv1075674copy number variation1nstd99human GRCh37 (hg19) chr9: 129,987,199-129,987,800 , GRCh38 (hg38) chr9: 127,224,920-127,225,521 GARNL3
    esv3621777copy number variation180estd214human GRCh37 (hg19) chr9: 130,033,124-130,034,800 , GRCh38 (hg38) chr9: 127,270,845-127,272,521 GARNL3
    esv3621778copy number variation1estd214human GRCh37 (hg19) chr9: 130,054,127-130,064,554 , GRCh38 (hg38) chr9: 127,291,848-127,302,275 GARNL3
    esv3621780copy number variation10estd214human GRCh37 (hg19) chr9: 130,109,659-130,110,239 , GRCh38 (hg38) chr9: 127,347,380-127,347,960 GARNL3
    esv3621779mobile element insertion120estd214human GRCh37 (hg19) chr9: 130,074,783-130,074,783 , GRCh38 (hg38) chr9: 127,312,504-127,312,504 GARNL3
    nsv1067806copy number variation5nstd101humanPathogenic NCBI36 (hg18) chr9: 194,193-140,193,718 , GRCh37 (hg19) chr9: 204,193-141,073,897 , GRCh38 (hg38) chr9: 193,412-138,179,445 TRH-GTG1-9, FOXD4L2, 1010 more genes
    nsv1052685copy number variation1nstd100human GRCh37 (hg19) chr9: 129,866,044-130,673,755 , GRCh38 (hg38) chr9: 127,103,765-127,911,476 , NCBI36 (hg18) chr9: 128,905,865-129,713,576 MIR2861, SH2D3C, 24 more genes
    nsv1045590copy number variation2nstd100human NCBI36 (hg18) chr9: 128,995,143-129,151,685 , GRCh37 (hg19) chr9: 129,955,322-130,111,864 , GRCh38 (hg38) chr9: 127,193,043-127,349,585 GARNL3, RALGPS1
    nsv1042177copy number variation1nstd100human NCBI36 (hg18) chr9: 129,065,108-129,119,506 , GRCh37 (hg19) chr9: 130,025,287-130,079,685 , GRCh38 (hg38) chr9: 127,263,008-127,317,406 GARNL3
    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
    nsv1031485copy number variation1nstd100human NCBI36 (hg18) chr9: 199,254-140,125,458 , GRCh37 (hg19) chr9: 209,254-141,005,637 , GRCh38 (hg38) chr9: 193,412-138,111,185 TRH-GTG1-9, FOXD4L2, 1010 more genes
    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, 1015 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, 1015 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, 704 more genes

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