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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2676879copy number variation198estd199human GRCh37 chr4: 34,779,980-34,829,038 , GRCh38.p12 chr4: 34,778,358-34,827,416 , GRCh38.p12 chr4|NW_003315915.1: 270,687-319,745 LOC105378262
    esv2665540copy number variation104estd199human GRCh37 chr22: 17,240,645-17,278,192 , GRCh38.p12 chr22: 16,759,755-16,797,302 XKR3
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2661219copy number variation458estd199human GRCh37 chr8: 48,180,445-48,214,692 , GRCh38.p12 chr8: 47,276,396-47,302,103 SPIDR
    esv2668535copy number variation54estd199human GRCh37 chr2: 19,185,645-19,225,292 , GRCh38.p12 chr2: 19,004,372-19,025,537 LINC01376
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2667772copy number variation1estd199human GRCh37 chr12: 57,156,832-57,174,623 , GRCh38.p12 chr12: 56,763,048-56,780,839 HSD17B6
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2670832copy number variation47estd199human GRCh37 chr3: 195,457,248-195,471,004 , GRCh38.p12 chr3|NT_187688.1: 50,599-64,322 , GRCh38.p12 chr3|NT_187689.1: 100,874-114,630 , GRCh38.p12 chr3|NT_187690.1: 50,598-64,329 , GRCh38.p12 chr3|NT_187691.1: 50,705-64,499 , GRCh38.p12 chr3|NT_187532.1: 100,874-114,630 , GRCh38.p12 chr3|NT_187649.1: 50,603-64,322 , GRCh38.p12 chr3: 195,730,377-195,744,133 , GRCh38.p12 chr3|NT_187678.1: 51,899-65,667 MUC20
    esv2675745copy number variation9estd199human GRCh37 chr21: 23,654,595-23,667,592 , GRCh38.p12 chr21: 22,282,275-22,295,272 , GRCh38.p12 chr21|NW_003315968.2: 186,504-199,501 LOC107985508
    esv2670748copy number variation204estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2670295copy number variation118estd199human GRCh37 chr3: 114,656,952-114,668,601 , GRCh38.p12 chr3: 114,938,105-114,949,754 ZBTB20
    esv2675519copy number variation112estd199human GRCh37 chr18: 66,745,594-66,756,999 , GRCh38.p12 chr18: 69,078,357-69,089,762 CCDC102B
    esv2663832copy number variation109estd199human GRCh37 chr4: 118,579,966-118,591,119 , GRCh38.p12 chr4: 117,658,811-117,669,964 LINC01378
    esv2659375copy number variation188estd199human GRCh37 chr21: 23,654,900-23,666,003 , GRCh38.p12 chr21: 22,282,580-22,293,683 , GRCh38.p12 chr21|NW_003315968.2: 186,809-197,912 LOC107985508
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2662536copy number variation311estd199human GRCh37 chr6: 72,863,851-72,873,540 , GRCh38.p12 chr6: 72,154,148-72,163,837 RIMS1
    esv2670098copy number variation35estd199human GRCh37 chr16: 76,661,500-76,671,078 , GRCh38.p12 chr16: 76,627,603-76,637,181 LINC02125
    esv2661768copy number variation445estd199human GRCh37 chr5: 12,811,019-12,820,535 , GRCh38.p12 chr5: 12,810,907-12,820,423 LOC105374657
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