NA18579 AND nstd20 - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv438248	copy number variation	1	nstd20	human		NCBI34 chr2: 29,611,575-29,629,488 , GRCh37.p13 chr2: 29,637,040-29,654,953 , GRCh38.p12 chr2: 29,414,174-29,432,087	ALK
nsv438259	copy number variation	1	nstd20	human		NCBI34 chr2: 30,137,687-30,155,192 , GRCh37.p13 chr2: 30,163,152-30,180,657 , GRCh38.p12 chr2: 29,940,286-29,957,791
nsv438237	copy number variation	1	nstd20	human		NCBI34 chr2: 29,386,658-29,401,473 , GRCh37.p13 chr2: 29,412,123-29,426,938 , GRCh38.p12 chr2: 29,189,257-29,204,072	ALK
nsv438270	copy number variation	1	nstd20	human		NCBI34 chr2: 30,230,147-30,242,577 , GRCh37.p13 chr2: 30,255,612-30,268,042 , GRCh38.p12 chr2: 30,032,746-30,045,176
nsv437907	copy number variation	146	nstd20	human		NCBI34 chr3: 194,196,286-194,205,086 , GRCh37.p13 chr3: 192,875,373-192,884,173 , GRCh38.p12 chr3: 193,157,584-193,166,384	VEZF1P1
nsv437903	copy number variation	23	nstd20	human		NCBI34 chr3: 191,058,267-191,060,542 , GRCh37.p13 chr3: 189,737,354-189,739,629 , GRCh38.p12 chr3: 190,019,565-190,021,840	P3H2
nsv438281	copy number variation	1	nstd20	human		GRCh38.p12 chr2: 30,184,036-30,195,428 , GRCh37.p13 chr2: 30,406,902-30,418,294 , NCBI34 chr2: 30,381,437-30,392,829	LOC105374414, SNORA10B
nsv438008	copy number variation	228	nstd20	human		NCBI34 chr7: 141,456,537-141,472,512 , GRCh38.p12 chr7\|NT_187562.1: 311,217-327,170 , GRCh37.p13 chr7\|NW_003571040.1: 491,288-507,241	TRB, TRBV6-2, 2 more genes
nsv437921	copy number variation	122	nstd20	human		GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN , NCBI34 chr4: 69,377,786-69,808,237	0
nsv437894	copy number variation	301	nstd20	human		NCBI34 chr3: 163,826,348-163,943,569 , GRCh37.p13 chr3: 162,505,435-162,622,656 , GRCh38.p12 chr3: 162,787,647-162,904,868	0
nsv438337	copy number variation	50	nstd20	human		NCBI34 chr2: 52,726,065-52,757,084 , GRCh37.p13 chr2: 52,751,531-52,782,550 , GRCh38.p12 chr2: 52,524,393-52,555,412	0
nsv438319	copy number variation	1	nstd20	human		NCBI34 chr21: 24,477,775-24,500,652 , GRCh37.p13 chr21: 25,555,904-25,578,781 , GRCh38.p12 chr21: 24,183,591-24,206,468	0
nsv438371	copy number variation	55	nstd20	human		NCBI34 chr2: 147,075,728-147,086,685 , GRCh37.p13 chr2: 146,864,959-146,875,916 , GRCh38.p12 chr2: 146,107,391-146,118,348	0
nsv438394	copy number variation	5	nstd20	human		NCBI34 chr3: 30,167,383-30,170,752 , GRCh37.p13 chr3: 30,192,418-30,195,787 , GRCh38.p12 chr3: 30,150,927-30,154,296	0
nsv438005	copy number variation	72	nstd20	human		NCBI34 chr7: 125,601,054-125,603,762 , GRCh37.p13 chr7: 126,046,565-126,049,273 , GRCh38.p12 chr7: 126,406,511-126,409,219	0
nsv437868	copy number variation	41	nstd20	human		NCBI34 chr3: 99,731,950-99,732,552 , GRCh37.p13 chr3: 98,411,049-98,411,651 , GRCh38.p12 chr3: 98,692,205-98,692,807	0
nsv438369	copy number variation	6	nstd20	human		NCBI34 chr2: 129,734,701-129,735,219 , GRCh37.p13 chr2: 129,641,434-129,641,952 , GRCh38.p12 chr2: 128,883,860-128,884,378	0

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