nhsl1[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3870706	copy number variation	1	nstd102	human	not provided	GRCh38 chr6: 138,588,771-138,608,297 , GRCh37 chr6: 138,909,908-138,929,434	NHSL1
esv3648329	copy number variation	1	estd216	human	not provided	GRCh37 chr6: 138,909,908-138,929,434 , GRCh38.p12 chr6: 138,588,771-138,608,297	NHSL1
nsv4350212	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374	NHSL1, LOC100131041, 146 more genes
nsv3904441	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 133,077,239-143,761,582 , GRCh38.p12 chr6: 132,756,100-143,440,445	NHSL1, SNORD101, 147 more genes
nsv3916499	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 136,359,437-146,708,473 , GRCh37.p13 chr6: 136,317,744-146,666,780 , GRCh38.p12 chr6: 135,996,606-146,345,644	NHSL1, SLC35D3, 127 more genes
nsv6314818	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 134,838,331-142,160,056 , GRCh37.p13 chr6: 135,159,469-142,481,193	NHSL1, PBOV1, 100 more genes
nsv6112726	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478	NHSL1, SIMALR, 99 more genes
nsv4675250	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 133,817,341-140,038,401 , GRCh38.p12 chr6: 133,496,203-139,717,264	NHSL1, ALDH8A1, 99 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	NHSL1, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	NHSL1, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	NHSL1, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	NHSL1, ITPR3, 2905 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	NHSL1, RNU6-770P, 810 more genes
nsv3911993	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033	NHSL1, LOC105369171, 418 more genes
nsv3915150	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038	NHSL1, KATNA1, 422 more genes
nsv3913689	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272	NHSL1, TPD52L1, 316 more genes
nsv3911164	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117	NHSL1, HYMAI, 263 more genes
nsv3924170	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 138,736,745-139,057,928 , GRCh37 chr6: 138,695,052-139,016,235 , GRCh38 chr6: 138,373,915-138,695,098	NHSL1, HEBP2, 5 more genes
nsv4685709	copy number variation	1	nstd102	human	not provided	GRCh37 chr6: 135,936,688-140,660,269 , GRCh38.p12 chr6: 135,615,550-140,339,132	NHSL1, MAP7, 74 more genes
nsv6313812	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 138,650,501-139,046,686 , GRCh38.p12 chr6: 138,329,364-138,725,549	NHSL1, NHSL1-AS1, 7 more genes

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Items: 20

Number of Variants: 20

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