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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3922684copy number variation2nstd102humanPathogenic GRCh38 (hg38) chr9: 193,412-138,179,445 , GRCh37.p13 chr9: 193,412-141,073,897 , NCBI36 (hg18) chr9: 183,412-140,193,718 NDUFA8, ABCA2, 2247 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr9: 203,861-138,125,937 , GRCh37.p13 chr9: 203,861-141,020,389 , NCBI36 (hg18) chr9: 193,861-140,140,210 NDUFA8, ABCA1, 2244 more genes
    nsv3920829copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr9: 121,112,395-138,075,224 , GRCh37.p13 chr9: 123,874,673-140,969,676 , NCBI36 (hg18) chr9: 122,914,494-140,089,497 NDUFA8, ASS1, 512 more genes
    nsv3920713copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr9: 203,862-138,125,937 , GRCh37.p13 chr9: 203,862-141,020,389 , NCBI36 (hg18) chr9: 193,862-140,140,210 NDUFA8, ABCA2, 2244 more genes
    nsv3919257copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr9: 204,193-138,179,445 , GRCh37.p13 chr9: 204,193-141,073,897 , NCBI36 (hg18) chr9: 194,193-140,193,718 NDUFA8, ALAD, 2246 more genes
    nsv3918439copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr9: 121,073,102-138,179,445 , GRCh37.p13 chr9: 123,835,380-141,073,897 , NCBI36 (hg18) chr9: 122,875,201-140,193,718 NDUFA8, ASS1, 515 more genes
    nsv3917022copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr9: 193,412-138,114,463 , GRCh37.p13 chr9: 193,412-141,008,915 , NCBI36 (hg18) chr9: 183,412-140,128,736 NDUFA8, ALAD, 2245 more genes
    nsv3916380copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr9: 193,412-138,124,532 , GRCh37.p13 chr9: 193,412-141,018,984 , NCBI36 (hg18) chr9: 183,412-140,138,805 NDUFA8, ABCA1, 2245 more genes
    nsv3915973copy number variation2nstd102humanPathogenic GRCh38 (hg38) chr9: 193,412-138,159,073 , GRCh37.p13 chr9: 193,412-141,053,525 , NCBI36 (hg18) chr9: 183,412-140,173,346 NDUFA8, ALAD, 2247 more genes
    nsv3915923copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 121,684,719-140,132,214 , GRCh37.p13 chr9: 122,644,898-141,012,393 , GRCh38.p12 chr9: 119,882,620-138,117,941 NDUFA8, ASS1, 529 more genes
    nsv3915468copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr9: 120,938,041-123,469,664 , GRCh37.p13 chr9: 123,700,319-126,231,943 , NCBI36 (hg18) chr9: 122,740,140-125,271,764 NDUFA8, STOM, 60 more genes
    nsv3912247copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981 NDUFA8, ABO, 2262 more genes
    nsv3911025copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr9: 193,412-138,124,524 , GRCh37.p13 chr9: 193,412-141,018,976 , NCBI36 (hg18) chr9: 183,412-140,138,797 NDUFA8, ABCA1, 2245 more genes
    nsv3907479copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955 , NCBI36 (hg18) chr9: 52,525-140,126,228 NDUFA8, ALAD, 2251 more genes
    nsv3906225copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr9: 124,642,754-141,146,461 , GRCh38.p12 chr9: 121,880,475-138,256,011 , NCBI36 (hg18) chr9: 123,682,575-140,266,282 NDUFA8, ASS1, 501 more genes
    nsv3905118copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645 , NCBI36 (hg18) chr9: 590-140,233,916 NDUFA8, ABL1, 2261 more genes
    nsv3900967copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664 , NCBI36 (hg18) chr9: 153,131-140,241,935 NDUFA8, ABCA2, 2251 more genes
    nsv3898141copy number variation1nstd102humanLikely pathogenic GRCh37 (hg19) chr9: 71,069,743-140,999,928 , GRCh38.p12 chr9: 68,454,827-138,105,476 , NCBI36 (hg18) chr9: 70,259,563-140,119,749 NDUFA8, ABCA1, 1356 more genes
    nsv3895453copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039 , NCBI36 (hg18) chr9: 36,587-140,186,312 NDUFA8, ABL1, 2253 more genes
    nsv3893142copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr9: 203,861-141,020,389 , GRCh38.p12 chr9: 203,861-138,125,937 , NCBI36 (hg18) chr9: 193,861-140,140,210 NDUFA8, AMBP, 2244 more genes
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