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Items: 1 to 20 of 89

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3902435copy number variation1nstd102humanBenign GRCh37 chr17: 43,912,490-43,912,786 , GRCh38.p12 chr17: 45,835,124-45,835,420 , GRCh38.p12 chr17|NT_187663.1: 537,246-537,542 LINC02210-CRHR1, CRHR1
    nsv3906712copy number variation1nstd102humanBenign GRCh37 chr17: 43,854,502-43,927,157 , GRCh38.p12 chr17: 45,777,136-45,849,791 , GRCh38.p12 chr17|NT_187663.1: 479,246-551,912 MAPT-AS1, SPPL2C, 2 more genes
    nsv4729736copy number variation1nstd102humanUncertain significance GRCh37 chr8: 67,066,779-67,162,066 , GRCh38.p12 chr8: 66,154,544-66,249,831 CRH, LINC00967, 3 more genes
    nsv6310311copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr17: 43,861,911-44,159,928 , GRCh38.p12 chr17: 45,784,545-46,082,562 , GRCh38.p12 chr17|NT_187663.1: 486,656-784,663 CRHR1, MAPT, 7 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3914262copy number variation1nstd102humanPathogenic GRCh37 chr8: 63,143,195-74,140,021 , GRCh38 chr8: 62,230,636-73,227,786 , NCBI36 chr8: 63,305,749-74,302,575 CRH, RRS1, 151 more genes
    nsv6290731copy number variation1nstd102humanPathogenic GRCh37 chr8: 66,045,954-69,807,260 , GRCh38.p12 chr8: 65,133,719-68,895,025 CRH, LINC00967, 64 more genes
    nsv3891386copy number variation1nstd102humanPathogenic GRCh37 chr8: 65,194,424-68,570,319 , GRCh38.p12 chr8: 64,281,867-67,658,084 CRH, MTATP6P12, 66 more genes
    nsv4456190copy number variation1nstd102humanPathogenic GRCh37 chr8: 65,280,508-67,782,846 , GRCh38.p12 chr8: 64,367,951-66,870,611 CRH, BHLHE22-AS1, 41 more genes
    nsv3915599copy number variation1nstd102humanPathogenic NCBI36 chr17: 41,012,476-42,049,627 , GRCh38 chr17: 45,579,327-46,661,960 , GRCh37 chr17: 43,656,693-44,694,311 LOC107985028, MAPT, 29 more genes
    nsv3909906copy number variation1nstd102humanPathogenic NCBI36 chr17: 41,062,678-42,117,723 , GRCh37.p13 chr17: 43,706,895-44,762,543 , GRCh38.p12 chr17: 45,629,529-46,685,177 MAPT-IT1, LOC105371802, 25 more genes
    nsv3912268copy number variation1nstd102humanPathogenic GRCh38 chr17: 45,629,520-46,661,960 , GRCh37 chr17: 43,706,886-44,694,283 , NCBI36 chr17: 41,062,669-42,049,599 LOC107985028, ARF2P, 25 more genes
    nsv3914891copy number variation1nstd102humanPathogenic NCBI36 chr17: 40,984,998-41,755,220 , GRCh37.p13 chr17: 43,629,215-44,399,455 , GRCh38.p12 chr17: 45,551,849-46,322,089 MAPK8IP1P2, LRRC37A, 25 more genes
    nsv4684193copy number variation1nstd102humanPathogenic GRCh37 chr17: 43,559,851-44,248,220 , GRCh38.p12 chr17|NT_187663.1: 172,640-872,959 , GRCh38.p12 chr17: 45,482,485-46,170,854 LOC105371800, KANSL1, 23 more genes
    nsv3919232copy number variation1nstd102humanPathogenic GRCh37 chr17: 43,651,731-44,351,152 , GRCh38 chr17: 45,574,365-46,273,786 , NCBI36 chr17: 41,007,514-41,706,929 DND1P2, DND1P1, 21 more genes
    nsv3923648copy number variation1nstd102humanPathogenic NCBI36 chr17: 41,009,010-41,707,421 , GRCh37 chr17: 43,653,227-44,351,644 , GRCh38 chr17: 45,575,861-46,274,278 ARL17B, LINC02210-CRHR1, 21 more genes
    nsv3922015copy number variation1nstd102humanPathogenic GRCh38 chr17: 45,516,110-46,211,895 , GRCh37 chr17: 43,593,476-44,224,221 , NCBI36 chr17: 40,949,259-41,645,038 LOC105376839, LOC105369225, 21 more genes
    nsv3919204copy number variation2nstd102humanPathogenic GRCh38 chr17: 45,578,381-46,273,786 , GRCh37 chr17: 43,655,747-44,351,152 , NCBI36 chr17: 41,011,530-41,706,929 LOC105371802, ARF2P, 21 more genes
    nsv3917363copy number variation1nstd102humanPathogenic NCBI36 chr17: 41,031,191-41,706,929 , GRCh38 chr17: 45,598,042-46,273,786 , GRCh37 chr17: 43,675,408-44,351,152 STH, LOC107985028, 19 more genes
    nsv3903631copy number variation1nstd102humanPathogenic GRCh37 chr17: 43,585,760-44,248,995 , GRCh38.p12 chr17: 45,508,394-46,171,629 , GRCh38.p12 chr17|NT_187663.1: 198,549-873,734 RPS26P8, LOC112267925, 22 more genes
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