rnpep[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3870964	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 201,952,244-201,959,490 , GRCh38.p12 chr1: 201,983,116-201,990,362	RNPEP
nsv3912840	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	RNPEP, CRB1, 1608 more genes
nsv3901050	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 200,144,603-203,112,078 , NCBI36 chr1: 198,380,354-201,347,829 , GRCh37 chr1: 200,113,731-203,081,206	RNPEP, IPO9, 80 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	RNPEP, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	RNPEP, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	RNPEP, RNU1-153P, 4887 more genes
nsv3918947	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	RNPEP, LOC101060227, 1608 more genes
nsv4450583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041	RNPEP, RGS18, 1186 more genes
nsv3881012	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801	RNPEP, LOC105372928, 1062 more genes
nsv6634372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485	RNPEP, LOC105373279, 1036 more genes
nsv3895767	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 187,143,981-224,299,417 , NCBI36 chr1: 185,379,736-222,553,742 , GRCh37 chr1: 187,113,113-224,487,119	RNPEP, LOC107985458, 590 more genes
nsv3889347	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 185,644,663-221,698,833 , GRCh38.p12 chr1: 185,675,531-221,525,491	RNPEP, MIR1231, 543 more genes
nsv6636965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906	RNPEP, PRELP, 527 more genes
nsv3879807	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 197,811,907-228,997,888 , GRCh38.p12 chr1: 197,842,777-228,862,141	RNPEP, RABIF, 637 more genes
nsv5381285	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699	RNPEP, DCST1, 2428 more genes
nsv4685577	copy number variation	1	nstd102	human	not provided	GRCh37 chr1: 194,356,425-210,988,710 , GRCh38.p12 chr1: 194,387,295-210,815,368	RNPEP, SEPTIN14P12, 332 more genes
nsv7095569	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922	RNPEP, TRK-TTT8-1, 228 more genes
nsv7095955	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435	RNPEP, ELF3, 189 more genes
nsv3905391	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 199,462,176-200,249,955 , GRCh37 chr1: 201,195,553-201,983,332 , GRCh38 chr1: 201,226,425-202,014,204	RNPEP, NAV1, 25 more genes

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rnpep[All Fields] AND 1[has_clinical] (20)
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