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  • The following term was not found in dbVar: Octopuses.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2878140insertion1nstd138pig Sscrofa10.2 (susScr3) chr5: 8,438,007-8,438,007 CSF2RB
    nsv2779429copy number variation5nstd135cow Bos_taurus_UMD_3.1 chr5: 75,699,059-76,269,946 , Bos_taurus_UMD_3.1.1 chr5: 75,699,059-76,269,946 , Btau_5.0.1 chr5: 75,913,502-76,482,305 MIR1835, IL2RB, 13 more genes
    nsv2778529copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr8: 90,717,375-91,029,121 , GRCh38 (hg38) chr8: 89,705,147-90,016,893 , NCBI36 (hg18) chr8: 90,786,497-91,098,297 DECR1, NBN, 2 more genes
    nsv2778243copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chr22: 35,674,826-39,466,442 , GRCh38 (hg38) chr22: 35,278,833-39,070,437 , NCBI36 (hg18) chr22: 34,004,826-37,796,388 HMGXB4, TOM1, 87 more genes
    nsv2778196copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr22: 21,025,654-22,336,268 , GRCh38 (hg38) chr22: 20,671,366-21,981,871 , NCBI36 (hg18) chr22: 19,355,654-20,666,268 MIR301B, RNA5SP493, 29 more genes
    nsv2778048copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr4: 174,478,959-175,855,409 , GRCh38 (hg38) chr4: 173,557,808-174,934,258 , NCBI36 (hg18) chr4: 174,715,534-176,091,984 MIR4276, LINC02269, 8 more genes
    nsv2777938copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chrX: 77,054,991-77,144,366 , GRCh38 (hg38) chrX: 77,799,494-77,888,869 , NCBI36 (hg18) chrX: 76,941,647-77,031,022 MAGT1
    nsv2777692copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr16: 84,776,177-85,087,145 , GRCh38 (hg38) chr16: 84,742,571-85,053,539 , NCBI36 (hg18) chr16: 83,333,678-83,644,646 LINC02176, ZDHHC7, 3 more genes
    nsv2777138copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr22: 17,008,132-49,591,432 , GRCh37 (hg19) chr22: 18,628,132-51,203,353 , GRCh38 (hg38) chr22: 18,145,365-50,806,138 DDTL, SNORD125, 595 more genes
    nsv2776533copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr5: 95,028,385-95,581,195 , GRCh38 (hg38) chr5: 95,692,681-96,245,491 , NCBI36 (hg18) chr5: 95,054,141-95,606,951 MIR583HG, LINC01554, 5 more genes
    nsv2776228copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr22: 16,054,691-51,237,463 , GRCh38 (hg38) chr22: 15,282,114-50,799,035 , NCBI36 (hg18) chr22: 14,434,691-49,584,329 DDTL, SNORD125, 623 more genes
    nsv2774182copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr16: 113,746-240,243 , GRCh38 (hg38) chr16: 63,748-190,244 , NCBI36 (hg18) chr16: 53,746-180,244 HBA1, HBA2, 7 more genes
    nsv2773876copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr22: 16,054,691-51,220,902 , GRCh38 (hg38) chr22: 15,282,114-50,782,474 , NCBI36 (hg18) chr22: 14,434,691-49,567,768 DDTL, SNORD125, 623 more genes
    nsv2773218copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr2: 86,286,136-86,516,984 , GRCh38 (hg38) chr2: 86,059,013-86,289,861 , NCBI36 (hg18) chr2: 86,139,647-86,370,495 MIR4779, IMMT, 5 more genes
    nsv2771518copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr22: 36,877,226-38,548,989 , GRCh38 (hg38) chr22: 36,481,179-38,152,982 , NCBI36 (hg18) chr22: 35,207,172-36,878,935 LL22NC01-81G9.3, MIR4534, 47 more genes
    nsv2770480copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr2: 77,520,872-78,259,733 , GRCh38 (hg38) chr2: 77,293,746-78,032,607 , NCBI36 (hg18) chr2: 77,374,380-78,113,241 SNAR-H, LINC01851, 1 more genes
    nsv2769800copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr22: 37,090,025-39,601,950 , GRCh38 (hg38) chr22: 36,693,980-39,205,945 , NCBI36 (hg18) chr22: 35,419,971-37,931,896 LL22NC01-81G9.3, MIR4534, 70 more genes
    nsv2768997copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr22: 16,888,900-51,197,838 , GRCh38 (hg38) chr22: 16,408,174-50,759,410 , NCBI36 (hg18) chr22: 15,268,900-49,544,704 DDTL, SNORD125, 618 more genes
    nsv2768533copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 8,093,169-11,881,742 , GRCh38 (hg38) chr8: 8,235,647-12,024,233 , NCBI36 (hg18) chr8: 8,130,579-11,919,151 MIR1322, MIR4286, 36 more genes
    nsv2136223short tandem repeat3nstd128human GRCh37 (hg19) chr22: 37,334,728-37,334,750 , GRCh38 (hg38) chr22: 36,938,686-36,938,708 CSF2RB
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